Tuberous sclerosis

Not to be confused with tuberculosis or TSC (disambiguation).

Tuberous sclerosis
Other names	Tuberous sclerosis complex (TSC), Bourneville disease, Bourneville-Pringle disease [1]
Main symptoms and signs of tuberous sclerosis
Specialty	Neurology, medical genetics
Prognosis	normal life expectancy
Frequency	7 to 12 per 100,000 [2]

Tuberous sclerosis complex (TSC) is a rare multisystem autosomal dominant genetic disease that causes non-cancerous tumours to grow in the brain and on other vital organs such as the kidneys, heart, liver, eyes, lungs and skin. A combination of symptoms may include seizures, intellectual disability, developmental delay, behavioral problems, skin abnormalities, lung disease, and kidney disease.

TSC is caused by a mutation of either of two genes, TSC1 and TSC2 , which code for the proteins hamartin and tuberin, respectively, with TSC2 mutations accounting for the majority and tending to cause more severe symptoms. ^[3] These proteins act as tumor growth suppressors, agents that regulate cell proliferation and differentiation. ^[4]

Prognosis is highly variable and depends on the symptoms, but life expectancy is normal for many. ^[4]

The prevalence of the disease is estimated to be 7 to 12 in 100,000. ^[2] The disease is often abbreviated to tuberous sclerosis, which refers to the hard swellings in the brains of patients, first described by French neurologist Désiré-Magloire Bourneville in 1880. ^[5]

Signs and symptoms

The physical manifestations of TSC are due to the formation of hamartia (malformed tissue such as the cortical tubers), hamartomas (benign growths such as facial angiofibroma and subependymal nodules), and very rarely, cancerous hamartoblastomas. The effect of these on the brain leads to neurological symptoms such as seizures, intellectual disability, developmental delay, and behavioral problems.^{[ citation needed ]}

Neurological

TSC in MRI

Three types of brain tumours are associated with TSC:^{[ citation needed ]}

• Giant cell astrocytoma: (grows and blocks the cerebrospinal fluid flow, leading to dilatation of ventricles causing headache and vomiting)
• Cortical tubers: after which the disease is named
• Subependymal nodules: form in the walls of ventricles

Classic intracranial manifestations of TSC include subependymal nodules and cortical/subcortical tubers. ^[6]

The tubers are typically triangular in configuration, with the apex pointed towards the ventricles, and are thought to represent foci of abnormal neuronal migration. The T2 signal abnormalities may subside in adulthood, but will still be visible on histopathological analysis. On magnetic resonance imaging (MRI), TSC patients can exhibit other signs consistent with abnormal neuron migration such as radial white matter tracts hyperintense on T2WI and heterotopic grey matter.^{[ citation needed ]}

Subependymal nodules are composed of abnormal, swollen glial cells and bizarre multinucleated cells which are indeterminate for glial or neuronal origin. Interposed neural tissue is not present. These nodules have a tendency to calcify as the patient ages. A nodule that markedly enhances and enlarges over time should be considered suspicious for transformation into a subependymal giant cell astrocytoma, which typically develops in the region of the foramen of Monro, in which case it is at risk of developing an obstructive hydrocephalus.

A variable degree of ventricular enlargement is seen, either obstructive (e.g. by a subependymal nodule in the region of the foramen of Monro) or idiopathic in nature.^{[ citation needed ]}

Neuropsychiatric

About 90% of people with TSC develop a range of neurodevelopmental, behavioural, psychiatric, and psychosocial difficulties. The "TSC‐associated neuropsychiatric disorders" are abbreviated TAND. These difficulties are less frequently identified and thus undertreated when compared with the neurological symptoms. ^[7] Most problems are associated with more severe intellectual delay or associated with childhood and adolescence, and some (for example depressed mood) may be unreported if the person is unable to communicate. TAND can be investigated and considered at six levels: behavioural, psychiatric, intellectual, academic, neuropsychological, and psychosocial. ^[7]

Behavioural problems most commonly seen include overactivity, impulsivity and sleeping difficulties. Also common are anxiety, mood swings, and severe aggression. Less common are depressed mood, self-injury, and compulsive behaviours. ^[7]

People with TSC are frequently also diagnosed with psychiatric disorders: autism spectrum disorder (ASD), attention deficit hyperactivity disorder (ADHD), anxiety disorder and depressive disorder. TSC is one of the most common genetic causes of autism spectrum disorder, which affects nearly half of people with TSC. ASD is more common in TSC2 than TSC1 and more common with earlier and more severe epilepsy, and with lower intellectual ability. ADHD is nearly as frequently seen in TSC as ASD (up to half of all people with TSC). Anxiety and depressive disorders, when they occur, are typically diagnosed in early adulthood and among those intellectually able to express their moods. ^[7]

The intellectual ability of people with TSC varies enormously. About 40–50% have a normal IQ. A normal IQ is much more commonly seen in TSC1 than TSC2, and profound intellectual disability seen in 34% of TSC2 compared with 10% of TSC1 in one study. Many studies have examined whether early onset, type and severity of epilepsy associates with intellectual ability. Academic issues occur even in people with TSC who have normal intellectual ability. These are often specific learning disorders such as dyscalculia (understanding mathematics), but also include other aspects affecting school life such as anxiety, lack of social skills or low self-esteem. ^[7]

About half of people with TSC, when assessed for neuropsychological skills, are in the bottom 5th percentile in some areas, which indicates a severe impairment. These include problems with attention (for example, being able to concentrate on two separate things like looking and listening), memory (particularly recall, verbal and spatial working memory) and executive function (for example, planning, self-monitoring, cognitive flexibility). ^[7]

The psychosocial impacts of TSC include low self-esteem and self-efficacy in the individual, and a burden on the family coping with a complex and unpredictable disorder. ^[7]

Kidneys

Computed tomography showing multiple angiomyolipomas of the kidney in a patient with lung lymphangioleiomyomatosis on CT: suspected TSC

Between 26% and 80% of TSC patients have benign tumors of the kidneys called angiomyolipomas, with hematuria being the most frequent presenting symptom. ^[8] TSC angiomyolipomas differ from non-TSC angiomyolipomas in age of presentation (31.5 years vs 53.6 years), mean tumor size (8.2 cm vs 4.5 cm), and percentage of cases requiring surgical intervention (50% vs 28%). ^[8] Although benign, an angiomyolipoma larger than 4 cm is at risk for a potentially catastrophic hemorrhage, either spontaneously or with minimal trauma.^{[ citation needed ]}

Lungs

Patients with TSC can develop progressive replacement of the lung parenchyma with multiple cysts, known as lymphangioleiomyomatosis (LAM). Recent genetic analysis has shown that the proliferative bronchiolar smooth muscle in TSC-related lymphangioleiomyomatosis is monoclonal metastasis from a coexisting renal angiomyolipoma. Cases of TSC-related lymphangioleiomyomatosis recurring following lung transplant have been reported. ^[9]

Heart

Small tumours of the heart muscle, called cardiac rhabdomyomas, are rare in the general population (perhaps 0.2% of children) but very common in people with TSC. Around 80% of children under two-years-old with TSC have at least one rhabdomyoma, and about 90% of those will have several. The vast majority of children with at least one rhabdomyoma, and nearly all children with multiple rhabdomyomas will be found to have TSC. Prenatal ultrasound, performed by an obstetric sonographer specializing in cardiology, can detect a rhabdomyoma after 20 weeks. Rhabdomyoma vary in size from a few millimetres to several centimetres, and are usually found in the lower chambers (ventricles) and less often in the upper chambers (atria). They grow in size during the second half of pregnancy, but regress after birth, and are seen in only around 20% of children over two years old. ^[10]

Most rhabdomyomas cause no problems but some may cause heart failure in the foetus or first year of life. Rhabdomyomas are believed to be responsible for the development of heart arrhythmia later in life, which is relatively common in TSC. Arrhythmia can be hard to spot in people with TSC, other than by performing routine ECG. For example, arrhythmia may cause fainting that is confused with drop seizures, and symptoms of arrhythmia such as palpitations may not be reported in an individual with developmental delay. ^[10]

Skin

A case of tuberous sclerosis showing facial angiofibromas in characteristic butterfly pattern.

From top to bottom: Hypopigmented macules, Shagreen patch and periungual fibroma of tuberous sclerosis.

Some form of dermatological sign is present in 96% of individuals with TSC. Most cause no problems, but are helpful in diagnosis. Some cases may cause disfigurement, necessitating treatment. The most common skin abnormalities include:

• Hypomelanic macules ("ash leaf spots") are present in about 90% of people with TSC. ^[11] These small white or lighter patches of skin may appear anywhere on the body, and are caused by a lack of melanin. They are usually the only visible sign of TSC at birth. In fair-skinned individuals, a Wood's lamp (ultraviolet light) may be required to see them. On the scalp, the effect may be a white patch of hair (poliosis). Patches smaller than 3mm are known as "confetti" skin lesions. ^[11]
• Facial angiofibromas are present in about 75% of people with TSC. ^[11] These are a rash of reddish spots or bumps on the nose and cheeks in a butterfly distribution, which consist of blood vessels and fibrous tissue. This potentially socially embarrassing rash starts to appear during childhood.^{[ citation needed ]}
• Ungual fibromas: Also known as Koenen's tumors, these are small fleshy tumors that grow around and under the toenails or fingernails. These are rare in childhood, but common by middle age. ^[12] They are generally more common on toes than on fingers, develop at 15–29 years, and are more common in women than in men.
• Fibrous cephalic plaques are present in about 25% of people with TSC. ^[11] These are raised, discoloured areas usually found on the forehead, but sometimes on the face or elsewhere on the scalp.^{[ citation needed ]}
• Shagreen patches are present in about half of people with TSC, appearing in childhood. ^[11] They are areas of thick leathery skin that are dimpled like an orange peel, and pigmented, they are usually found on the lower back or nape of the neck, or scattered across the trunk or thighs. The frequency of these lesions rises with age.^{[ citation needed ]}
• Dental enamel pits are found in almost all adults with TSC. ^[11]
• Intraoral fibromas are small surface-tumours found in the gums, inside the cheeks or tongue. Gum (gingival) fibromas are found in about 20-50% of people with TSC, more commonly in adults. ^[11]

Eyes

Retinal lesions, called astrocytic hamartomas (or "phakomas"), which appear as a greyish or yellowish-white lesion in the back of the globe on the ophthalmic examination. Astrocytic hamartomas can calcify, and they are in the differential diagnosis of a calcified globe mass on a CT scan. ^[13]

Nonretinal lesions associated with TSC include:

• Coloboma ^[13]
• Angiofibromas of the eyelids ^[13]
• Papilledema (related to hydrocephalus)^{[ citation needed ]}

Pancreas

Pancreatic neuroendocrine tumours have been described in rare cases of TSC. ^[14]

Variability

Individuals with TSC may experience none or all of the clinical signs discussed above. The following table shows the prevalence of some of the clinical signs in individuals diagnosed with TSC.

The frequency of signs in children with TSC, grouped by age

Genetics

TSC is inherited in an autosomal dominant fashion.

TSC is a genetic disorder with an autosomal dominant pattern of inheritance, variable expressivity, and incomplete penetrance. ^{[12] [16]} Two-thirds of TSC cases result from sporadic genetic mutations, not inheritance, but their offspring may inherit it from them. Current genetic tests have difficulty locating the mutation in roughly 20% of individuals diagnosed with the disease. So far, it has been mapped to two genetic loci, TSC1 and TSC2 . ^[17]

TSC1 encodes for the protein hamartin, is located on chromosome 9 q34, and was discovered in 1997. ^[18] TSC2 encodes for the protein tuberin, is located on chromosome 16 p13.3, and was discovered in 1993. ^[19] TSC2 is contiguous with PKD1, the gene involved in one form of polycystic kidney disease (PKD). Gross deletions affecting both genes may account for the 2% of individuals with TSC who also develop polycystic kidney disease in childhood. ^[20] TSC2 has been associated with a more severe form of TSC. ^[21] However, the difference is subtle and cannot be used to identify the mutation clinically. Estimates of the proportion of TSC caused by TSC2 range from 55% to 90%. ^[3]

TSC1 and TSC2 are both tumor suppressor genes that function according to Knudson's "two hit" hypothesis. That is, a second random mutation must occur before a tumor can develop. This explains why, despite its high penetrance, TSC has wide expressivity.^{[ citation needed ]}

Hamartin Identifiers Symbol TSC1 NCBI gene 7248 HGNC 12362 OMIM 605284 RefSeq NM_000368 UniProt Q92574 Other data Locus Chr. 9 q34 Search for Structures Swiss-model Domains InterPro

Tuberin Identifiers Symbol TSC2 NCBI gene 7249 HGNC 12363 OMIM 191092 RefSeq NM_000548 UniProt P49815 Other data Locus Chr. 16 p13.3 Search for Structures Swiss-model Domains InterPro

Pathophysiology

Hamartin and tuberin function as a complex which is involved in the control of cell growth and cell division. The complex appears to interact with RHEB GTPase, thus sequestering it from activating mTOR signalling, part of the growth factor (insulin) signalling pathway. Thus, mutations at the TSC1 and TSC2 loci result in a loss of control of cell growth and cell division, and therefore a predisposition to forming tumors. TSC affects tissues from different germ layers. Cutaneous and visceral lesions may occur, including angiofibroma, cardiac rhabdomyomas, and renal angiomyolipomas. The central nervous system lesions seen in this disorder include hamartomas of the cortex, hamartomas of the ventricular walls, and subependymal giant cell tumors, which typically develop in the vicinity of the foramina of Monro.^{[ citation needed ]}

Molecular genetic studies have defined at least two loci for TSC. In TSC1, the abnormality is localized on chromosome 9q34, but the nature of the gene protein, called hamartin, remains unclear. No missense mutations occur in TSC1. In TSC2, the gene abnormalities are on chromosome 16p13. This gene encodes tuberin, a guanosine triphosphatase–activating protein. The specific function of this protein is unknown. In TSC2, all types of mutations have been reported; new mutations occur frequently. Few differences have yet been observed in the clinical phenotypes of patients with mutation of one gene or the other.^{[ citation needed ]}

Cells from individuals with pathogenic mutations in the TSC2 gene display abnormal accumulation of glycogen that is associated with depletion of lysosomes and autophagic impairment. The defective degradation of glycogen by the autophagy-lysosome pathway is, at least in part, independent of impaired regulation of mTORC1 and is restored, in cultured cells, by the combined use of PKB/Akt and mTORC1 pharmacological inhibitors. ^[22]

Diagnosis

Tuberous sclerosis complex is diagnosed with clinical and genetic tests. There are many different mutations in the TSC1 and TSC2 genes that have been identified in individuals with TSC. A pathogenic mutation in the gene prevents the proteins from being made or inactivates the proteins. If such a pathogenic mutation is found then this alone is sufficient to diagnose TSC. However, some mutations are less clear in their effect, and so not sufficient alone for diagnosis. Between 1 in 10 and 1 in 4 of individuals with TSC have no mutation that can be identified. Once a particular mutation is identified in someone with TSC, this mutation can be used to make confident diagnoses in other family members. ^[11]

For clinical diagnosis, there isn't one sign that is unique (pathognomonic) to TSC, nor are all signs seen in all individuals. Therefore, several signs are considered together, classed as either major or minor features. An individual with two major features, or one major feature and at least two minor features can be given a definite diagnosis of TSC. If only one major feature or at least two minor features are present, the diagnosis is only regarded as possibly TSC. ^[11]

Diagnostic Criteria for Tuberous Sclerosis Complex ^[11]

Major Features
	Location	Sign	Onset [23]	Note
1	Skin	Hypomelanotic macules	Infant – child	At least three, at least 5 mm in diameter.
2	Head	Facial angiofibromas or fibrous cephalic plaque	Infant – adult	At least three angiofibromas
3	Fingers and toes	Ungual fibroma	Adolescent – adult	At least two
4	Skin	Shagreen patch (connective tissue nevus)	Child
5	Eyes	Multiple retinal nodular hamartomas	Infant
6	Brain	Cortical dysplasias	Fetus	(includes tubers and cerebral white matter radial migration lines)
7	Brain	Subependymal nodule	Child – adolescent
8	Brain	Subependymal giant cell astrocytoma	Child – adolescent
9	Heart	Cardiac rhabdomyoma	Fetus
10	Lungs	Lymphangioleiomyomatosis	Adolescent – adult
11	Kidneys	Renal angiomyolipoma	Child – adult	At least two. Together, 10 and 11 count as one major feature.
Minor Features
	Location	Sign		Note
1	Skin	"Confetti" skin lesions
2	Teeth	Dental enamel pits		At least three
3	Gums	Intraoral fibromas		At least two
4	Eyes	Retinal achromic patch
5	Kidneys	Multiple renal cysts
6	Liver, spleen and other organs	Nonrenal hamartoma

TSC can be first diagnosed at any stage of life. Prenatal diagnosis is possible by chance if heart tumours are discovered during routine ultrasound. In infancy, epilepsy, particularly infantile spasms, or developmental delay may lead to neurological tests. The white patches on the skin may also first become noticed. In childhood, behavioural problems and autism spectrum disorder may provoke a diagnosis. During adolescence, the skin problems appear. In adulthood, kidney and lung problems may develop. An individual may also be diagnosed at any time as a result of genetic testing of family members of another affected person. ^[24]

Management

Tuberous sclerosis complex affects multiple organ systems so a multidisciplinary team of medical professionals is required.^{[ citation needed ]}

In suspected or newly diagnosed TSC, the following tests and procedures are recommended by 2012 International Tuberous Sclerosis Complex Consensus Conference. ^[25]

• Take a personal and family history covering three generations. Genetic counselling and tests determine if other individuals are at risk.
• A magnetic resonance imaging (MRI) of the brain to identify tubers, subependymal nodules (SEN) and sub-ependymal giant cell astrocytomas (SEGA).
• Children undergo a baseline electroencephalograph (EEG) and family educated to identify seizures if/when they occur.
• Assess children for behavioural issues, autism spectrum disorder, psychiatric disorders, developmental delay, and neuropsychological problems.
• Scan the abdomen for tumours in various organs, but most importantly angiomyolipomata in the kidneys. MRI is superior to CT or ultrasound. Take blood pressure and test renal function.
• In adult women, test pulmonary function and perform a high-resolution computed tomography (HRCT) of the chest.
• Examine the skin under a Wood's lamp (hypomelanotic macules), the fingers and toes (ungual fibroma), the face (angiofibromas), and the mouth (dental pits and gingival fibromas).
• In infants under three, perform an echocardiogram to spot rhabdomyomas, and electrocardiogram (ECG) for any arrhythmia.
• Use a fundoscope to spot retinal hamartomas or achromic patches.

The various symptoms and complications from TSC may appear throughout life, requiring continued surveillance and adjustment to treatments. The following ongoing tests and procedures are recommended by 2012 International Tuberous Sclerosis Complex Consensus Conference. ^[25]

• In children and adults younger than 25 years, a magnetic resonance imaging (MRI) of the brain is performed every one to three years to monitor for subependymal giant cell astrocytoma (SEGA). If a SEGA is large, growing or interfering with ventricles, the MRI is performed more frequently. After 25 years, if there are no SEGAs then periodic scans may no longer be required. A SEGA causing acute symptoms are removed with surgery, otherwise either surgery or drug treatment with an mTOR inhibitor may be indicated.
• Repeat screening for TSC-associated neuropsychiatric disorders (TAND) at least annually. Sudden behavioural changes may indicate a new physical problem (for example with the kidneys, epilepsy or a SEGA).
• Routine EEG determined by clinical need.
• Infantile spasms are best treated with vigabatrin and adrenocorticotropic hormone used as a second-line therapy. Other seizure types have no TSC-specific recommendation, though epilepsy in TSC is typically difficult to treat (medically refractory).
• Repeat MRI of abdomen every one to three years throughout life. Check renal (kidney) function annually. Should angiomyolipoma bleed, this is best treated with embolisation and then corticosteroids. Removal of the kidney (nephrectomy) is strongly to be avoided. An asymptomatic angiomyolipoma that is growing larger than 3 cm is best treated with an mTOR inhibitor drug. Other renal complications spotted by imaging include polycystic kidney disease and renal cell carcinoma.
• Repeat chest HRCT in adult women every five to 10 years. Evidence of lymphangioleiomyomatosis (LAM) indicates more frequent testing. An mTOR inhibitor drug can help, though a lung transplant may be required.
• A 12-lead ECG should be performed every three to five years.

The mTOR inhibitor everolimus was approved in the US for treatment of TSC-related tumors in the brain (subependymal giant cell astrocytoma) in 2010 and in the kidneys (renal angiomyolipoma) in 2012. ^{[26] [27]}   Oral everolimus (rapalog) reduces tumour size, is effective in terms of response to skin lesions and does not increase the risk of adverse events. ^[28] Everolimus also showed evidence of effectiveness at treating epilepsy in some people with TSC. ^{[29] [30]} In 2017, the European Commission approved everolimus for treatment of refractory partial-onset seizures associated with TSC. ^[31]

Neurosurgical intervention may reduce the severity and frequency of seizures in TSC patients. ^{[32] [33]} Embolization and other surgical interventions can be used to treat renal angiomyolipoma with acute hemorrhage. Surgical treatments for symptoms of lymphangioleiomyomatosis (LAM) in adult TSC patients include pleurodesis to prevent pneumothorax and lung transplantation in the case of irreversible lung failure. ^[25]

Other treatments that have been used to treat TSC manifestations and symptoms include a ketogenic diet for intractable epilepsy and pulmonary rehabilitation for LAM. ^[34] Facial angiofibromas can be reduced with laser treatment and the effectiveness of mTOR inhibitor topical treatment is being investigated. Laser therapy is painful, requires anaesthesia, and has risks of scarring and dyspigmentation. ^[35]

Prognosis

The prognosis for individuals with TSC depends on the severity of symptoms, which range from mild skin abnormalities to varying degrees of learning disabilities and epilepsy to severe intellectual disability, uncontrollable seizures, and kidney failure. Those individuals with mild symptoms generally do well and live long, productive lives, while individuals with the more severe form may have serious disabilities. However, with appropriate medical care, most individuals with the disorder can look forward to normal life expectancy. ^[4]

A study of 30 TSC patients in Egypt found, "...earlier age of seizures commencement (<6 months) is associated with poor seizure outcome and poor intellectual capabilities. Infantile spasms and severely epileptogenic EEG patterns are related to the poor seizure outcome, poor intellectual capabilities and autistic behavior. Higher tubers numbers is associated with poor seizure outcome and autistic behavior. Left-sided tuber burden is associated with poor intellect, while frontal location is more encountered in ASD [ autism spectrum disorders]. So, close follow up for the mental development and early control of seizures are recommended in a trial to reduce the risk factors of poor outcome. Also early diagnosis of autism will allow for earlier treatment and the potential for better outcome for children with TSC." ^[36]

Leading causes of death include renal disease, brain tumour, lymphangioleiomyomatosis of the lung, and status epilepticus or bronchopneumonia in those with severe intellectual disability. ^[37] Cardiac failure due to rhabdomyomas is a risk in the fetus or neonate but is rarely a problem subsequently. Kidney complications such as angiomyolipoma and cysts are common and more frequent in females than males and in TSC2 than TSC1. Renal cell carcinoma is uncommon. Lymphangioleiomyomatosis is only a risk for females with angiomyolipomas. ^[38] In the brain, the subependymal nodules occasionally degenerate to subependymal giant cell astrocytomas. These may block the circulation of cerebrospinal fluid around the brain, leading to hydrocephalus.^{[ citation needed ]}

Detection of the disease should be followed by genetic counselling. It is also important to realize that though the disease does not have a cure, symptoms can be treated symptomatically. Hence, awareness regarding different organ manifestations of TSC is important. ^[39]

Epidemiology

TSC occurs in all races and ethnic groups, and in both sexes. The live-birth prevalence is estimated to be between 10 and 16 cases per 100,000. A 1998 study ^[2] estimated total population prevalence between about 7 and 12 cases per 100,000, with more than half of these cases undetected. Prior to the invention of CT scanning to identify the nodules and tubers in the brain, the prevalence was thought to be much lower, and the disease associated with those people diagnosed clinically with learning disability, seizures and facial angiofibroma. Whilst still regarded as a rare disease, TSC is common when compared to many other genetic diseases, with at least 1 million individuals affected worldwide. ^[15]

History

Main article: Timeline of tuberous sclerosis

Désiré-Magloire Bourneville

TSC first came to medical attention when dermatologists described the distinctive facial rash (1835 and 1850). A more complete case was presented by von Recklinghausen (1862), who identified heart and brain tumours in a newborn who had only briefly lived. However, Bourneville (1880) is credited with having first characterized the disease, coining the name "tuberous sclerosis", thus earning the eponym Bourneville's disease. The neurologist Vogt (1908) established a diagnostic triad of epilepsy, idiocy, and adenoma sebaceum (an obsolete term for facial angiofibroma). ^[40]

Symptoms were periodically added to the clinical picture. The disease as presently understood was first fully described by Gomez (1979). The invention of medical ultrasound, CT and MRI has allowed physicians to examine the internal organs of live patients and greatly improved diagnostic ability.^{[ citation needed ]}

In 2002, treatment with rapamycin was found to be effective at shrinking tumours in animals. This has led to human trials of rapamycin as a drug to treat several of the tumors associated with TSC. ^[41]

See also

• Characteristics of syndromic ASD conditions

References

1. Islam, Monica P.; Roach, E. Steve (2015). "Tuberous sclerosis complex". Neurocutaneous Syndromes. Handbook of Clinical Neurology. Vol. 132. pp. 97–109. doi:10.1016/B978-0-444-62702-5.00006-8. ISBN   9780444627025. PMID   26564073.
2. O'Callaghan FJ, Shiell AW, Osborne JP, Martyn CN (May 1998). "Prevalence of tuberous sclerosis estimated by capture-recapture analysis". Lancet. 351 (9114): 1490. doi:10.1016/S0140-6736(05)78872-3. PMID   9605811. S2CID   9262685.
3. Rendtorff ND, Bjerregaard B, Frödin M, Kjaergaard S, Hove H, Skovby F, Brøndum-Nielsen K, Schwartz M (October 2005). "Analysis of 65 tuberous sclerosis complex (TSC) patients by TSC2 DGGE, TSC1/TSC2 MLPA, and TSC1 long-range PCR sequencing, and report of 28 novel mutations". Human Mutation. 26 (4): 374–83. doi: 10.1002/humu.20227 . PMID   16114042. S2CID   10571695.
4. "Tuberous Sclerosis Fact Sheet". National Institute of Neurological Disorders and Stroke. 6 July 2018. Retrieved 16 December 2018.
5. Brigo F, Lattanzi S, Trinka E, Nardone R, Bragazzi NL, Ruggieri M, et al. (December 2018). "First descriptions of tuberous sclerosis by Désiré-Magloire Bourneville (1840-1909)". Neuropathology. 38 (6): 577–582. doi:10.1111/neup.12515. PMID   30215888. S2CID   52269610.
6. Ridler K, Suckling J, Higgins N, Bolton P, Bullmore E (September 2004). "Standardized whole brain mapping of tubers and subependymal nodules in tuberous sclerosis complex". Journal of Child Neurology. 19 (9): 658–65. doi:10.1177/08830738040190090501. PMID   15563011. S2CID   23176067.
7. de Vries PJ, Wilde L, de Vries MC, Moavero R, Pearson DA, Curatolo P (September 2018). "A clinical update on tuberous sclerosis complex-associated neuropsychiatric disorders (TAND)". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 178 (3): 309–320. doi:10.1002/ajmg.c.31637. PMC   6209538 . PMID   30117265.
8. Lendvay, Thomas S.; Marshall, Fray F. (May 2003). "The Tuberous Sclerosis Complex and its Highly Variable Manifestations". Journal of Urology. 169 (5): 1635–1642. doi:10.1097/01.ju.0000058253.40352.60. ISSN   0022-5347. PMID   12686801.
9. Henske EP (December 2003). "Metastasis of benign tumor cells in tuberous sclerosis complex". Genes, Chromosomes & Cancer. 38 (4): 376–81. doi:10.1002/gcc.10252. PMID   14566858. S2CID   22211249.
10. Hinton RB, Prakash A, Romp RL, Krueger DA, Knilans TK (November 2014). "Cardiovascular manifestations of tuberous sclerosis complex and summary of the revised diagnostic criteria and surveillance and management recommendations from the International Tuberous Sclerosis Consensus Group". Journal of the American Heart Association. 3 (6): e001493. doi:10.1161/JAHA.114.001493. PMC   4338742 . PMID   25424575.
11. Northrup H, Krueger DA (October 2013). "Tuberous sclerosis complex diagnostic criteria update: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference". Pediatric Neurology. 49 (4): 243–54. doi:10.1016/j.pediatrneurol.2013.08.001. PMC   4080684 . PMID   24053982.
12. Northrup H, Koenig MK, Pearson DA, Au KS (1993). "Tuberous Sclerosis Complex". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A (eds.). GeneReviews. Seattle (WA): University of Washington. PMID   20301399.
13. Randle SC (April 2017). "Tuberous Sclerosis Complex: A Review". Pediatric Annals. 46 (4): e166–e171. doi:10.3928/19382359-20170320-01. PMID   28414398.
14. Arva NC, Pappas JG, Bhatla T, Raetz EA, Macari M, Ginsburg HB, Hajdu CH (January 2012). "Well-differentiated pancreatic neuroendocrine carcinoma in tuberous sclerosis--case report and review of the literature". The American Journal of Surgical Pathology. 36 (1): 149–53. doi:10.1097/PAS.0b013e31823d0560. PMID   22173120.
15. Curatolo P, ed. (2003). "Diagnostic Criteria". Tuberous Sclerosis Complex: From Basic Science to Clinical Phenotypes. International review of child neurology. London: Mac Keith Press. ISBN   978-1-898683-39-1. OCLC   53124670.
16. Baraitser M, Patton MA (February 1985). "Reduced penetrance in tuberous sclerosis". Journal of Medical Genetics. 22 (1): 29–31. doi:10.1136/jmg.22.1.29. PMC   1049373 . PMID   3981577.
17. Young J, Povey S (July 1998). "The genetic basis of tuberous sclerosis". Molecular Medicine Today. 4 (7): 313–9. doi:10.1016/S1357-4310(98)01245-3. PMID   9743993.
18. van Slegtenhorst M, de Hoogt R, Hermans C, Nellist M, Janssen B, Verhoef S, et al. (August 1997). "Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34". Science. 277 (5327): 805–808. doi:10.1126/science.277.5327.805. PMID   9242607.
19. European Chromosome 16 Tuberous Sclerosis Consortium (December 1993). "Identification and characterization of the tuberous sclerosis gene on chromosome 16". Cell. 75 (7): 1305–15. doi:10.1016/0092-8674(93)90618-Z. PMID   8269512. S2CID   29476292.
20. Brook-Carter PT, Peral B, Ward CJ, Thompson P, Hughes J, Maheshwar MM, Nellist M, Gamble V, Harris PC, Sampson JR (December 1994). "Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease--a contiguous gene syndrome". Nature Genetics. 8 (4): 328–32. doi:10.1038/ng1294-328. PMID   7894481. S2CID   23793670.
21. Dabora SL, Jozwiak S, Franz DN, Roberts PS, Nieto A, Chung J, Choy YS, Reeve MP, Thiele E, Egelhoff JC, Kasprzyk-Obara J, Domanska-Pakiela D, Kwiatkowski DJ (January 2001). "Mutational analysis in a cohort of 224 tuberous sclerosis patients indicates increased severity of TSC2, compared with TSC1, disease in multiple organs". American Journal of Human Genetics. 68 (1): 64–80. doi:10.1086/316951. PMC   1234935 . PMID   11112665.
22. Pal R, Xiong Y, Sardiello M (February 2019). "Abnormal glycogen storage in tuberous sclerosis complex caused by impairment of mTORC1-dependent and -independent signaling pathways". Proc Natl Acad Sci U S A. 116 (8): 2977–2986. Bibcode:2019PNAS..116.2977P. doi: 10.1073/pnas.1812943116 . PMC   6386676 . PMID   30728291.
23. Crino PB, Nathanson KL, Henske EP (September 2006). "The tuberous sclerosis complex". The New England Journal of Medicine. 355 (13): 1345–56. CiteSeerX   10.1.1.319.8438 . doi:10.1056/NEJMra055323. PMID   17005952.
24. "Tuberous Sclerosis Complex". University Hospitals Birmingham NHS Foundation Trust. Archived from the original on 16 December 2018. Retrieved 16 December 2018.
25. Krueger DA, Northrup H (October 2013). "Tuberous sclerosis complex surveillance and management: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference". Pediatric Neurology. 49 (4): 255–65. doi:10.1016/j.pediatrneurol.2013.08.002. PMC   4058297 . PMID   24053983.
26. "Press Announcements - FDA approves Afinitor for non-cancerous kidney tumors caused by rare genetic disease". www.fda.gov. Retrieved 8 February 2017.
27. "FDA Approval for Everolimus". National Cancer Institute. 21 April 2009. Archived from the original on 11 February 2017. Retrieved 8 February 2017.
28. Sasongko TH, Kademane K, Chai Soon Hou S, Jocelyn TX, Zabidi-Hussin Z (July 2023). "Rapamycin and rapalogs for tuberous sclerosis complex". The Cochrane Database of Systematic Reviews. 2023 (7): CD011272. doi:10.1002/14651858.CD011272.pub3. PMC  10334695. PMID   37432030.
29. French JA, Lawson JA, Yapici Z, Ikeda H, Polster T, Nabbout R, et al. (October 2016). "Adjunctive everolimus therapy for treatment-resistant focal-onset seizures associated with tuberous sclerosis (EXIST-3): a phase 3, randomised, double-blind, placebo-controlled study". Lancet. 388 (10056): 2153–2163. doi: 10.1016/s0140-6736(16)31419-2 . PMID   27613521.
30. Capal JK, Franz DN (2016). "Profile of everolimus in the treatment of tuberous sclerosis complex: an evidence-based review of its place in therapy". Neuropsychiatric Disease and Treatment. 12: 2165–2172. doi: 10.2147/NDT.S91248 . PMC   5003595 . PMID   27601910.
31. Novartis International AG. "Novartis drug Votubia® receives EU approval to treat refractory partial-onset seizures in patients with TSC". GlobeNewswire News Room. Retrieved 8 February 2017.
32. Asano E, Juhász C, Shah A, Muzik O, Chugani DC, Shah J, Sood S, Chugani HT (July 2005). "Origin and propagation of epileptic spasms delineated on electrocorticography". Epilepsia. 46 (7): 1086–97. doi:10.1111/j.1528-1167.2005.05205.x. PMC   1360692 . PMID   16026561.
33. Chugani HT, Luat AF, Kumar A, Govindan R, Pawlik K, Asano E (August 2013). "α-[11C]-Methyl-L-tryptophan--PET in 191 patients with tuberous sclerosis complex". Neurology. 81 (7): 674–80. doi:10.1212/WNL.0b013e3182a08f3f. PMC   3775695 . PMID   23851963.
34. Hong AM, Turner Z, Hamdy RF, Kossoff EH (August 2010). "Infantile spasms treated with the ketogenic diet: prospective single-center experience in 104 consecutive infants". Epilepsia. 51 (8): 1403–407. doi: 10.1111/j.1528-1167.2010.02586.x . PMID   20477843. S2CID   26666421.
35. Jacks SK, Witman PM (September–October 2015). "Tuberous Sclerosis Complex: An Update for Dermatologists". Pediatric Dermatology. 32 (5): 563–70. doi:10.1111/pde.12567. PMID   25776100. S2CID   72874.
36. Samir H, Ghaffar HA, Nasr M (March 2011). "Seizures and intellectual outcome: clinico-radiological study of 30 Egyptian cases of tuberous sclerosis complex". European Journal of Paediatric Neurology. 15 (2): 131–37. doi:10.1016/j.ejpn.2010.07.010. PMID   20817577.
37. Shepherd CW, Gomez MR, Lie JT, Crowson CS (August 1991). "Causes of death in patients with tuberous sclerosis". Mayo Clinic Proceedings. 66 (8): 792–96. doi:10.1016/s0025-6196(12)61196-3. PMID   1861550.
38. Rakowski SK, Winterkorn EB, Paul E, Steele DJ, Halpern EF, Thiele EA (November 2006). "Renal manifestations of tuberous sclerosis complex: Incidence, prognosis, and predictive factors". Kidney International. 70 (10): 1777–82. doi: 10.1038/sj.ki.5001853 . PMID   17003820.
39. Amin, S; Kingswood, J C; Bolton, P F; Elmslie, F; Gale, D P; Harland, C; Johnson, S R; Parker, A; Sampson, J R; Smeaton, M; Wright, I; O’Callaghan, F J (2019). "The UK guidelines for management and surveillance of Tuberous Sclerosis Complex". QJM: An International Journal of Medicine. 112 (3): 171–182. doi:10.1093/qjmed/hcy215. ISSN   1460-2725.
40. Curatolo P, ed. (2003). "Historical Background". Tuberous Sclerosis Complex: From Basic Science to Clinical Phenotypes. International review of child neurology. London: Mac Keith Press. ISBN   978-1-898683-39-1. OCLC   53124670.
41. Rott HD, Mayer K, Walther B, Wienecke R (March 2005). "Zur Geschichte der Tuberösen Sklerose (The History of Tuberous Sclerosis)" (PDF) (in German). Tuberöse Sklerose Deutschland e.V. Archived from the original (PDF) on 15 March 2007. Retrieved 8 January 2007.

External links

• tuberous-sclerosis at NIH / UW GeneTests
• GeneReview/NCBI/NIH/UW entry on Tuberous Sclerosis Complex