Epidermolysis bullosa

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Epidermolysis bullosa
Other namesButterfly children [1]
Iraqi-boy-epidermolysis bullosa-090216-M-8096M-001.jpg
A five-year-old boy with epidermolysis bullosa
Specialty Dermatology
Symptoms Painful skin blisters [2] [3]
Complications Esophageal narrowing, squamous cell skin cancer, amputations [4] [5]
Usual onsetAt birth [5]
DurationOften lifelong [5]
Types Epidermolysis bullosa simplex, dystrophic epidermolysis bullosa, junctional epidermolysis bullosa, Kindler syndrome [2]
Causes Genetic [2]
Diagnostic method Skin biopsy, genetic testing [6]
Differential diagnosis Bullous pemphigoid, pemphigus vulgaris, friction blisters, insect bites [5]
Treatment Wound care, pain control, controlling infections, nutritional support [2]
Prognosis Death usually occurs during early adulthood
Frequencyaround 1 in 500,000 [5]

Epidermolysis bullosa (EB) is a group of rare medical conditions that result in easy blistering of the skin and mucous membranes. Blisters occur with minor trauma or friction and are painful. Its severity can range from mild to fatal. [7] Inherited EB is a rare disease with a prevalence in the United States of 8.2 per million live births. [8] Those with mild cases may not develop symptoms until they start to crawl or walk. Complications may include esophageal narrowing, squamous cell skin cancer, and the need for amputations.[ medical citation needed ]

Contents

EB is due to a mutation in at least one of 16 different genes. Some types are autosomal dominant while others are autosomal recessive. [2] The underlying mechanism is a defect in attachment between or within the layers of the skin. Loss or diminished function of type VII collagen leads to weakness in the structural architecture of the dermal–epidermal junction (DEJ) and mucosal membranes. [9] There are four main types: epidermolysis bullosa simplex (EBS), dystrophic epidermolysis bullosa (DEB), junctional epidermolysis bullosa (JEB), and Kindler syndrome. The diagnosis is suspected based on symptoms and confirmed by skin biopsy or genetic testing.

There is no cure for the condition. Management involves wound care, pain control, controlling infections, nutritional support, and prevention and treatment of complications. [7] About half a million people are affected globally. [5] It occurs equally commonly in males and females. [10]

Classification

Epidermolysis bullosa refers to a group of disorders that involve the formation of blisters following trivial trauma. Over 300 mutations have been identified in this condition. [11] They have been classified into the following types: [12] [13] : 596 

Epidermolysis bullosa simplex

Epidermolysis bullosa simplex (EBS) is a form of EB that causes blisters at the site of rubbing. It typically affects the hands and feet, and is typically inherited in an autosomal dominant manner, affecting the keratin genes KRT5 and KRT14. Therefore, there is a failure in keratinization, which affects the integrity and the ability of the skin to resist mechanical stresses.[ citation needed ]

Junctional epidermolysis bullosa

Junctional epidermolysis bullosa (JEB) is an inherited disease affecting laminin and collagen. This disease is characterized by blister formation within the lamina lucida of the basement membrane zone [13] : 599  and is inherited in an autosomal recessive manner. It also presents with blisters at the site of friction, especially on the hands and feet, and has variants that can occur in children and adults. Less than one person per million people is estimated to have this form of EB. [14]

Dystrophic epidermolysis bullosa

Dystrophic epidermolysis bullosa (DEB) is an inherited variant affecting the skin and other organs. DEB is caused by genetic defects (or mutations) within the human COL7A1 gene encoding the protein type VII collagen (collagen VII). [15] DEB-causing mutations can be either autosomal dominant or autosomal recessive. Epidermis bullosa pruriginosa and albopapuloid epidermolysis bullosa (Pasini's disease) are rare subtypes of this disease. [16]

Other genetic

OMIM NameLocusGene
609638 epidermolysis bullosa, lethal acantholytic 6p24 DSP

Epidermolysis bullosa acquisita

Acral peeling

Pathophysiology

The human skin consists of two layers: an outermost layer called the epidermis and a layer underneath called the dermis. In individuals with healthy skin, there are protein anchors between these two layers (Dermo epidermal junction) that prevent them from moving independently from one another (shearing). In people born with EB, the two skin layers lack the protein anchors that hold them together, resulting in extremely fragile skin—even minor mechanical friction (like rubbing or pressure) or trauma will separate the layers of the skin and form blisters and painful sores. [17] EB  individuals manifest unremitting skin blistering that evolves into chronic wounds, inflammation, and fibrosis. [18] People with EB have compared the sores with third-degree burns. Furthermore, as a complication of the chronic skin damage, people with EB have an increased risk of malignancies (cancers) of the skin. [19] Virtually any organ lined or covered by epithelium may be injured in inherited EB. External eye, esophagus, upper airway, and genitourinary tract are the epithelial surfaced tissues that are at particular risk. [20]

Diagnosis

EB can be diagnosed either by a skin (punch) biopsy at the edge of a wound with immunofluorescent mapping, or via blood sample and genetic testing.[ citation needed ]

Treatment

Treatment of the epidermolysis bullosa by transplantation of laminin5 modified stem cells Treatment of the epidermolysis bullosa by transplantation of laminin5 modified stem cells..jpg
Treatment of the epidermolysis bullosa by transplantation of laminin5 modified stem cells

Research has focused on changing the mixture of keratins produced in the skin. There are 54 known keratin genes—of which 28 belong to the type I intermediate filament genes and 26 to type II—which work as heterodimers. Many of these genes share substantial structural and functional similarity, but they are specialized to cell type and/or conditions under which they are normally produced. If the balance of production could be shifted away from the mutated, dysfunctional keratin gene toward an intact keratin gene, symptoms could be reduced. For example, sulforaphane, a compound found in broccoli, was found to reduce blistering in a mouse model to the point where affected pups could not be identified visually, when injected into pregnant mice (5 μmol/day = 0.9 mg) and applied topically to newborns (1 μmol/day = 0.2 mg in jojoba oil). [21]

As of 2008 clinical research at the University of Minnesota has explored allogeneic bone marrow transplantation for RD and junctional EB, treating a two-year-old child who is one of two brothers with EB. A second transplant has also been performed on the child's older brother. A Missouri boy has also successfully undergone the transplant, as well as a 5 year old boy from Alabama. So far there have been 12 successful transplants. [22] Another transplant is scheduled for a California baby. A clinical trial is planned for 30 subjects. [23] However, the immune suppression that bone marrow transplantation requires causes a risk of serious infections with large scale blisters and skin erosion. [24] Indeed, at least four people have died in the course of either preparation for or institution of bone marrow transplantation for EB, out of only a small group of patients treated so far. [24] The mechanism of action of this therapy is unclear as hematopoietic stem cells are not thought to contribute to epithelial lineages. Rather, it is speculated that cross-correction from tissue-resident graft-derived immune cells contributes to the observed clinical benefit. [25]

A pilot study performed in 2015 suggests that systemic granulocyte-colony stimulating factor (G-CSF) may promote increased wound healing in people with dystrophic EB. [26] Transplanting skin derived from genetically modified stem cells onto the wound surfaces has been studied with a report of improvements in one person. [27]

A 2017 clinical trial with male RDEB (recessive dystrophic EB) patients conducted successful grafting of type VII gene corrected keratinocytes (COL7A1 gene correction using retrovirus transduction), without any serious adverse effects. Type VII collage formation was observed at the dermis-epidermis junction in significant amounts. [28]

A 2020 study demonstrated the safe allogenic grafting of acellular dermal matrix/scaffolds in EB patients without any observed infection or necrosis and instead noted fewer required dressing changes, promoted wound healing, pain reduction, and an overall improvement in the quality of life of the patients. [29]

In 2022, a pharmaceutical gel made out of birch bark extract from Betula pendula and Betula pubescens was approved by the European Union as a treatment for epidermolysis bullosa. [30] [31]

Monitoring

The Epidermolysis Bullosa Disease Activity and Scarring index (EBDASI) is a scoring system that objectively quantifies the severity of EB. The EBDASI is a tool for clinicians and patients to monitor the severity of the disease. It has also been designed to evaluate the response to new therapies for the treatment of EB. The EBDASI was developed and validated by Professor Dedee Murrell and her team of students and fellows at the St George Hospital, University of New South Wales, in Sydney, Australia. It was presented at the International Investigative Dermatology congress in Edinburgh in 2013 and a paper-based version was published in the Journal of the American Academy of Dermatology in 2014. [32]

Prognosis

A 2014 study classified cases into three types—EBS, JEB and DEB—and reviewed their times of death. The first two types tended to die in infancy and the last in early adulthood. [33] In a survey of 11 families affected by the disease, lack of awareness of the disease by both the public and health care providers raised concerns about the care provided. [5]

Epidemiology

An estimated 20 per million live births are diagnosed with EB, [34] and 9 per million people in the general population have the condition. Of these cases, approximately 92% are EBS, 5% are DEB, 1% are JEB, and 2% are unclassified. Carrier frequency ranges from 1 in 333 for JEB, to 1 in 450 for DEB; the carrier frequency for EBS is presumed to be much higher than JEB or DEB.[ citation needed ]

The disorder occurs in every racial and ethnic group and affects both sexes. [35] [36]

Society and culture

In 2010, Emma Fogarty, a campaigner for DEBRA Ireland (the EB charity), was awarded a People of the Year Award. [37] Actor Colin Farrell has campaigned with Fogarty on behalf of affected people. [38]

In 2014, Pearl Jam lead vocalist Eddie Vedder together with his wife Jill McCormick co-founded the EB Research Partnership, [39] a non-profit organization dedicated to finding a cure for EB. [40] McCormick is childhood friends with Ryan Fullmer, whose son, Michael, was born with EB. Vedder, McCormick, Ryan Fullmer, and his wife, Heather founded Heal EB. In 2014, they merged Heal EB with the Jackson Gabriel Research Foundation to create the EB Research Partnership. The EBRP hosts several annual fundraising events. To date, they have raised $12 million to fund research to find a cure. [41]

On March 1, 2019, heavyweight boxer Luis Ortiz was named an honorary ambassador for the EB community by the EB Research Partnership. Ortiz's daughter, Lismercedes, was born with EB. [42]

Canadian television personality Liz Trinnear has spoken publicly about her struggles with the condition. [43]

Movies

The condition was brought to public attention in 2004 in the UK through the Channel 4 documentary The Boy Whose Skin Fell Off, chronicling the life and death of Jonny Kennedy, an Englishman with EB. [44] In the United States, HBO ran a documentary, My Flesh and Blood , in 2003.[ citation needed ] Additionally, the film Butterfly Girl follows Abigail Evans with the disease. [45] In Canada, The Sports Network's award-winning documentary on Jonathan Pitre led to extensive coverage on the boy's disease, treatment, and death. [46] [47]

Other names

Other terms used to describe those affected include "butterfly children" as the skin is fragile as a butterfly's wings, [48] "cotton wool babies", [49] [50] or "crystal skin children". [51]

Related Research Articles

Type II keratins constitutes the Type II intermediate filaments (IFs) of the intracytoplasmatic cytoskeleton, which is present in all mammalian epithelial cells. The type 2 cytokeratins consist of basic or neutral, high molecular weight proteins which in vivo are arranged in pairs of heterotypic Type I and Type II keratin chains, coexpressed during differentiation of simple and stratified epithelial tissues. It has been seen that Type II Keratins are developed before Type 1 keratins during human embryonic development.

<span class="mw-page-title-main">Keratin 14</span> Protein-coding gene in the species Homo sapiens

Keratin 14 is a member of the type I keratin family of intermediate filament proteins. Keratin 14 was the first type I keratin sequence determined. Keratin 14 is also known as cytokeratin-14 (CK-14) or keratin-14 (KRT14). In humans it is encoded by the KRT14 gene.

<span class="mw-page-title-main">Hemidesmosome</span>

Hemidesmosomes are very small stud-like structures found in keratinocytes of the epidermis of skin that attach to the extracellular matrix. They are similar in form to desmosomes when visualized by electron microscopy, however, desmosomes attach to adjacent cells. Hemidesmosomes are also comparable to focal adhesions, as they both attach cells to the extracellular matrix. Instead of desmogleins and desmocollins in the extracellular space, hemidesmosomes utilize integrins. Hemidesmosomes are found in epithelial cells connecting the basal epithelial cells to the lamina lucida, which is part of the basal lamina. Hemidesmosomes are also involved in signaling pathways, such as keratinocyte migration or carcinoma cell intrusion.

<span class="mw-page-title-main">Palmoplantar keratoderma</span> Medical condition

Palmoplantar keratodermas are a heterogeneous group of disorders characterized by abnormal thickening of the stratum corneum of the palms and soles.

DEBRA is the name of an international medical research charity dedicated to securing effective drug treatments and ultimately cures for every type of epidermolysis bullosa, with national groups in over 40 countries including in the United Kingdom and the United States.

Jonny Kennedy was a British man who had a rare inherited condition known as dystrophic epidermolysis bullosa. Kennedy ultimately died of skin cancer, a complication of EB.

<span class="mw-page-title-main">Epidermolysis bullosa simplex</span> Medical condition

Epidermolysis bullosa simplex (EBS) is a disorder resulting from mutations in the genes encoding keratin 5 or keratin 14.

<span class="mw-page-title-main">Kindler syndrome</span> Medical condition

Kindler syndrome is a rare congenital disease of the skin caused by a mutation in the KIND1 gene.

<span class="mw-page-title-main">Keratin 5</span>

Keratin 5, also known as KRT5, K5, or CK5, is a protein that is encoded in humans by the KRT5 gene. It dimerizes with keratin 14 and forms the intermediate filaments (IF) that make up the cytoskeleton of basal epithelial cells. This protein is involved in several diseases including epidermolysis bullosa simplex and breast and lung cancers.

<span class="mw-page-title-main">Junctional epidermolysis bullosa (veterinary medicine)</span> Genetic disorder of horses

Junctional epidermolysis bullosa (JEB) is an inherited disorder that is also known as red foot disease or hairless foal syndrome. JEB is the result of a genetic mutation that inhibits protein production that is essential for skin adhesion. Therefore, tissues, such as skin and mouth epithelia, are affected. Blisters form over the entire body causing pain and discomfort, and open sores leave newborn foals highly susceptible to secondary infection. The condition can be categorized into two types of mutations: JEB1 and JEB2. JEB1 is found in Belgian Draft horses, as well as other related Draft breeds. In contrast, JEB2 is found in American Saddlebred horses.

<span class="mw-page-title-main">Collagen, type XVII, alpha 1</span> Mammalian protein found in humans

Collagen XVII, previously called BP180, is a transmembrane protein which plays a critical role in maintaining the linkage between the intracellular and the extracellular structural elements involved in epidermal adhesion, identified by Diaz and colleagues in 1990.

<span class="mw-page-title-main">Epidermolysis bullosa dystrophica</span> Medical condition

Epidermolysis bullosa dystrophica or dystrophic EB (DEB) is an inherited disease affecting the skin and other organs.

<span class="mw-page-title-main">Genodermatosis</span> Medical condition

Genodermatosis is a hereditary skin disease with three inherited modes including single gene inheritance, multiple gene inheritance and chromosome inheritance. There are many different types of genodermatosis, the prevalence of genodermatosis ranges from 1 per 6000 people to 1 per 500,000 people. Genodermatosis has influence on the texture, color and structure of skin cuticle and connective tissue, specific lesion site and clinical manifestations on the body vary depending on the type. In the spite of the variety and complexity of genodermatosis, there are still some common methods that can help people diagnose. After diagnosis, different types of genodermatosis require different levels of therapy including interventions, nursing interventions and treatments. Among that, research of therapy for some new, complex and rare types are still in the developing stage. The impact of genodermatosis not only can be seen in body but also can be seen in all aspects of patients' life, including but not limited to psychological, family life, economic conditions and social activities. Accordingly, the patients need treatment, support and help in these areas.

<span class="mw-page-title-main">Collagen, type VII, alpha 1</span> Protein found in humans

Collagen alpha-1(VII) chain is a protein that in humans is encoded by the COL7A1 gene. It is composed of a triple helical, collagenous domain flanked by two non-collagenous domains, and functions as an anchoring fibril between the dermal-epidermal junction in the basement membrane. Mutations in COL7A1 cause all types of dystrophic epidermolysis bullosa, and the exact mutations vary based on the specific type or subtype. It has been shown that interactions between the NC-1 domain of collagen VII and several other proteins, including laminin-5 and collagen IV, contribute greatly to the overall stability of the basement membrane.

Anchoring fibrils extend from the basal lamina of epithelial cells and attach to the lamina reticularis by wrapping around the reticular fiber bundles. The basal lamina and lamina reticularis together make up the basement membrane. Anchoring fibrils are essential to the functional integrity of the dermoepidermal junction.

Bart syndrome, also known as aplasia cutis congenita type VI, is a rare genetic disorder characterized by the association of congenital localized absence of skin, mucocutaneous blistering and absent and dystrophic nails.

Junctional epidermolysis bullosa is a skin condition characterized by blister formation within the lamina lucida of the basement membrane zone.

Transient bullous dermolysis of the newborn (TBDN) is a skin condition that presents in newborns. It is characterized by blister formation secondary to even mild trauma.

A coma blister, or coma bullae, is a skin lesion or blister that typically arises due to pressure in an individual with impaired consciousness. They vary in size, ranging from 4 to 5 centimeters in diameter, and may appear hemorrhagic or blood filled. Coma blisters are usually found in the extremities and trunk. These types of blisters have been associated with the overdose of central nervous system (CNS) depressants especially barbiturates, but also tricyclic antidepressants, hypnotics, benzodiazepines, opiates, antipsychotics, and alcohol. However, studies have found that coma blisters are not caused by the toxicity of these drugs, but due to hypoxia and external pressure on the comatose individual's skin from being immobilized. Coma blisters have been frequently found on individuals who have overdosed on drugs, but have also been found on individuals with chronic kidney failure, hypercalcemia, diabetic ketoacidosis, and a variety of neurologic conditions. Coma blisters are more frequent in adults and less common among children as demonstrated by the few cases published in literature.

Scioderm, acquired by Amicus Therapeutics in 2015, was a rare disease company focused on developing a treatment for Epidermolysis Bullosa (EB), a rare genetic disease characterized by extremely fragile skin and recurrent blister formation. There are currently no approved therapies for EB. Scioderm was developing a topical treatment known as SD-101, or Zorblisa, aimed at triggering wound reduction and closure, and a reduction in body surface area coverage of blisters and lesions.

References

  1. ↑ Fine, Jo-David; Hintner, Helmut (2009). Life with Epidermolysis Bullosa (EB): Etiology, Diagnosis, Multidisciplinary Care and Therapy. Springer Science & Business Media. p. 242. ISBN   9783211792711. Archived from the original on 2021-11-03. Retrieved 2020-11-21.
  2. 1 2 3 4 5 "Epidermolysis bullosa". rarediseases.info.nih.gov. Archived from the original on 16 May 2018. Retrieved 16 May 2018.
  3. ↑ "Epidermolysis Bullosa". National Institute of Arthritis and Musculoskeletal and Skin Diseases. 11 April 2017. Archived from the original on 4 October 2017. Retrieved 16 May 2018.
  4. ↑ "Epidermolysis Bullosa". National Institute of Arthritis and Musculoskeletal and Skin Diseases. 11 April 2017. Archived from the original on 4 October 2017. Retrieved 16 May 2018.
  5. 1 2 3 4 5 6 7 Tabor, A; Pergolizzi JV, Jr; Marti, G; Harmon, J; Cohen, B; Lequang, JA (May 2017). "Raising Awareness Among Healthcare Providers about Epidermolysis Bullosa and Advancing Toward a Cure". The Journal of Clinical and Aesthetic Dermatology. 10 (5): 36–48. PMC   5479476 . PMID   28670357.
  6. ↑ "Epidermolysis Bullosa". National Institute of Arthritis and Musculoskeletal and Skin Diseases. 11 April 2017. Archived from the original on 4 October 2017. Retrieved 16 May 2018.
  7. 1 2 Bardhan, Ajoy; Bruckner-Tuderman, Leena; Chapple, Iain L. C.; Fine, Jo-David; Harper, Natasha; Has, Cristina; Magin, Thomas M.; Marinkovich, M. Peter; Marshall, John F.; McGrath, John A.; Mellerio, Jemima E. (2020-09-24). "Epidermolysis bullosa". Nature Reviews Disease Primers. 6 (1): 78. doi:10.1038/s41572-020-0210-0. ISSN   2056-676X. PMID   32973163. S2CID   221861310. Archived from the original on 2020-11-18. Retrieved 2020-09-26.
  8. ↑ FINE, JO-DAVID; JOHNSON, LORRAINE B.; WEINER, MADELINE; STEIN, AMY; CASH, SARAH; DeLEOZ, JOY; DEVRIES, DAVID T.; SUCHINDRAN, CHIRAYATH (November 2004). "Genitourinary Complications of Inherited Epidermolysis Bullosa: Experience of the National Epidermylosis Bullosa Registry and Review of the Literature". Journal of Urology. 172 (5): 2040–2044. doi:10.1097/01.ju.0000143200.86683.2c. PMID   15540785.
  9. ↑ Vanden Oever, Michael; Twaroski, Kirk; Osborn, Mark J; Wagner, John E; Tolar, Jakub (2017-11-01). "Inside out: regenerative medicine for recessive dystrophic epidermolysis bullosa". Pediatric Research. 83 (1–2): 318–324. doi: 10.1038/pr.2017.244 . ISSN   0031-3998. PMID   29593249. S2CID   4447720.
  10. ↑ "Epidermolysis Bullosa". National Institute of Arthritis and Musculoskeletal and Skin Diseases. 11 April 2017. Archived from the original on 4 October 2017. Retrieved 16 May 2018.
  11. ↑ Koshida, S.; Tsukamura, A.; Yanagi, T.; Nakahara, S.; Takeuchi, Y.; Kato, T.; Tanaka, T.; Nakano, H.; Shimizu, H. (2013). "Hallopeau-Siemens dystrophic epidermolysis bullosa due to homozygous 5818delC mutation in the COL7A gene". Pediatr Int. 55 (2): 234–7. doi:10.1111/j.1442-200X.2012.03638.x. PMID   23679163. S2CID   24238328.
  12. ↑ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN   0-7216-2921-0.
  13. 1 2 Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN   0-07-138076-0.
  14. ↑ "Junctional epidermolysis bullosa". Genetics Home Reference. NIH. Archived from the original on 12 October 2013. Retrieved 11 October 2013.
  15. ↑ Varki, Roslyn; Sadowski, Sara; Uitto, Jouni; Pfendner, Ellen (2007-03-01). "Epidermolysis bullosa. II. Type VII collagen mutations and phenotype–genotype correlations in the dystrophic subtypes". Journal of Medical Genetics. 44 (3): 181–192. doi:10.1136/jmg.2006.045302. ISSN   0022-2593. PMC   2598021 . PMID   16971478.
  16. ↑ McGRATH, J.a.; Schofield, O.m.v.; Eady, R.a.j. (1994-05-01). "Epidermolysis bullosa pruriginosa: dystrophic epidermolysis bullosa with distinctive clinicopathological features". British Journal of Dermatology. 130 (5): 617–625. doi:10.1111/j.1365-2133.1994.tb13109.x. ISSN   1365-2133. PMID   8204470. S2CID   5958915.
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  18. ↑ Cianfarani, Francesca; Zambruno, Giovanna; Castiglia, Daniele; Odorisio, Teresa (July 2017). "Pathomechanisms of Altered Wound Healing in Recessive Dystrophic Epidermolysis Bullosa". The American Journal of Pathology. 187 (7): 1445–1453. doi: 10.1016/j.ajpath.2017.03.003 . ISSN   0002-9440. PMID   28460207.
  19. ↑ Mallipeddi, R. (November 2002). "Epidermolysis bullosa and cancer". Clinical and Experimental Dermatology. 27 (8): 616–623. doi:10.1046/j.1365-2230.2002.01130.x. ISSN   0307-6938. PMID   12472531. S2CID   40006559. Archived from the original on 2022-03-08. Retrieved 2022-03-08.
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  21. ↑ Kerns, Michelle L.; DePianto, Daryle; Dinkova-Kostova, Albena T.; Talalay, Paul; Coulombe, Pierre A. (2007-09-04). "Reprogramming of keratin biosynthesis by sulforaphane restores skin integrity in epidermolysis bullosa simplex". Proceedings of the National Academy of Sciences. 104 (36): 14460–14465. Bibcode:2007PNAS..10414460K. doi: 10.1073/pnas.0706486104 . ISSN   0027-8424. PMC   1964870 . PMID   17724334.
  22. ↑ "My Skin is Killing Me - Epidermolysis Bullosa | Extraordinary People Documentary | Reel Truth". YouTube .
  23. ↑ Josephine Marcotty (2008-07-03). "Long-shot stem-cell treatment gives two brothers a future". Star Tribune. Archived from the original on 2009-02-11. Retrieved 2008-07-22.
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  25. ↑ Wagner, John E.; Ishida-Yamamoto, Akemi; McGrath, John A.; Hordinsky, Maria; Keene, Douglas R.; Riddle, Megan J.; Osborn, Mark J.; Lund, Troy; Dolan, Michelle; Blazar, Bruce R.; Tolar, Jakub (2010-08-12). "Bone Marrow Transplantation for Recessive Dystrophic Epidermolysis Bullosa". The New England Journal of Medicine. 363 (7): 629–639. doi:10.1056/NEJMoa0910501. ISSN   0028-4793. PMC   2967187 . PMID   20818854.
  26. ↑ Fine, Jo-David; Manes, Becky; Frangoul, Haydar (July 2015). "Systemic granulocyte colony-stimulating factor (G-CSF) enhances wound healing in dystrophic epidermolysis bullosa (DEB): Results of a pilot trial". Journal of the American Academy of Dermatology. 73 (1): 56–61. doi:10.1016/j.jaad.2015.04.015. ISSN   0190-9622. PMID   25956659.
  27. ↑ Hirsch, T; Rothoeft, T; Teig, N; Bauer, JW; Pellegrini, G; De Rosa, L; Scaglione, D; Reichelt, J; Klausegger, A; Kneisz, D; Romano, O; Secone Seconetti, A; Contin, R; Enzo, E; Jurman, I; Carulli, S; Jacobsen, F; Luecke, T; Lehnhardt, M; Fischer, M; Kueckelhaus, M; Quaglino, D; Morgante, M; Bicciato, S; Bondanza, S; De Luca, M (16 November 2017). "Regeneration of the entire human epidermis using transgenic stem cells". Nature. 551 (7680): 327–332. Bibcode:2017Natur.551..327H. doi:10.1038/nature24487. PMC   6283270 . PMID   29144448.
  28. ↑ Siprashvili, Zurab; Nguyen, Ngon T.; Gorell, Emily S.; Loutit, Kylie; Khuu, Phuong; Furukawa, Louise K.; Lorenz, H. Peter; Leung, Thomas H.; Keene, Douglas R.; Rieger, Kerri E.; Khavari, Paul (2016-11-01). "Safety and Wound Outcomes Following Genetically Corrected Autologous Epidermal Grafts in Patients With Recessive Dystrophic Epidermolysis Bullosa". JAMA. 316 (17): 1808–1817. doi:10.1001/jama.2016.15588. ISSN   1538-3598. PMID   27802546. Archived from the original on 2022-03-08. Retrieved 2022-03-08.
  29. ↑ Pliszczyński, J.; Nita, M.; Kowalewski, C.; Woźniak, K.; Eljaszewicz, A.; Moniuszko, M.; Kamiński, A.; Śladowski, D.; Zimek, Z.; Majewski, S.; Kosieradzki, M. (September 2020). "Transplantation of a New Biological Product in Rare Diseases, Such as Epidermolysis Bullosa: Response and Clinical Outcome". Transplantation Proceedings. 52 (7): 2239–2243. doi:10.1016/j.transproceed.2020.02.119. ISSN   1873-2623. PMID   32334796. S2CID   216555379. Archived from the original on 2022-03-08. Retrieved 2022-03-08.
  30. ↑ "Filsuvez EPAR". European Medicines Agency (EMA). 13 April 2022. Archived from the original on 6 July 2022. Retrieved 6 July 2022. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  31. ↑ "European Commission Approves Filsuvez for the treatment of Dystrophic and Junctional EB" (Press release). Amryt Pharma plc. 23 June 2022. Archived from the original on 23 June 2022. Retrieved 6 July 2022.
  32. ↑ Development, reliability, and validity of a novel Epidermolysis Bullosa Disease Activity and Scarring index (EBDASI). 2014. Loh CH, Kim J, Su JC, Daniel BS, Venugopal SS, Rhodes LM, Intong LR, Law MG, Murrell DF. January 2014. JAAD, 70, 1pp.
  33. ↑ Hon, Kam Lun Ellis; Li, Joshua J.; Cheng, Bernadette L.; Luk, David C.; Murrell, Dedee F.; Choi, Paul C. L.; Leung, Alexander K. C. (2015-03-04). "Age and etiology of childhood epidermolysis bullosa mortality". Journal of Dermatological Treatment. 26 (2): 178–182. doi:10.3109/09546634.2014.915002. ISSN   0954-6634. PMID   24724596. S2CID   33722635.
  34. ↑ "Epidermolysis Bullosa Clinic Frequently Asked Questions". Stanford Medicine — Dermatology. Archived from the original on 8 March 2018. Retrieved 13 April 2018.
  35. ↑ Marinkovich, MP; Wells, MJ; Perry, V; James, WD; Ortonne, JP (December 3, 2007). "Epidermolysis Bullosa". Bullous Diseases. emedicine.com. Archived from the original on 2008-10-25. Retrieved 2008-07-22.
  36. ↑ Pfendner, Ellen; Uitto, Jouni; Fine, Jo-David (2000-11-07). "Epidermolysis Bullosa Carrier Frequencies in the US Population". Journal of Investigative Dermatology. 116 (3): 483–484. doi: 10.1046/j.1523-1747.2001.127911.x . PMID   11231335.
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  38. ↑ Townsend, Michelle (21 December 2018). "Late Late Show viewers praise Colin Farrell and EB sufferer Emma Fogarty for honest interview". RSVP live. Archived from the original on 22 December 2018.
  39. ↑ "Board of Directors - EB Research Partnership". ebresearch.org. Archived from the original on 2019-03-27. Retrieved 2019-03-22.
  40. ↑ Reed, Ryan (2014-10-10). "Eddie Vedder Supports Research for Curing Rare Skin Disease EB". Rolling Stone. Archived from the original on 2019-03-22. Retrieved 2019-03-22.
  41. ↑ Lee, Kate (November 11, 2016). "Eddie Vedder and the Chicago Cubs Team Up to Raise $50,000 to Help Kids with EB". Medium. Archived from the original on March 22, 2019. Retrieved March 22, 2019.
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  43. ↑ Melissa Greer, "Liz Trinnear On The Rare Skin Condition That Made Her Who She Is Today". Best Health, February 19, 2019.
  44. ↑ "Series 1 - The Boy Whose Skin Fell Off". Channel 4. 2004. Archived from the original on 2016-04-28. Retrieved 2009-02-28.
  45. ↑ "Butterfly Girl: Remembering Abigail Evans". The Austinot. January 12, 2015. Archived from the original on 2017-07-13.
  46. ↑ Andrew Duffy, "TSN documentary on Jonathan Pitre wins screen award". Ottawa Citizen. March 9, 2016. Archived from the original on 6 April 2018. Retrieved 6 April 2018.
  47. ↑ "Ottawa boy Jonathan Pitre dead at 17 from rare skin disease". CBC News. April 6, 2018. Archived from the original on 2018-04-08.
  48. ↑ Roddy Isles; Head of Press (2005-05-12). "Dundee Scientists on road to cure for "Butterfly Children" condition". University of Dundee. Archived from the original on 2014-01-04. Retrieved 2008-07-22.
  49. ↑ Suellen Hinde; Health reporter (2006-11-26). "Little girl's life of pain". HeraldSun.com.au. Archived from the original on 2008-09-22. Retrieved 2008-07-22.
  50. ↑ Robyn Gobert, Past President of DEBRA Australia Inc. (May 2002). "Times change - A family's story about living with EB". e-bility.com. Archived from the original on 2008-07-03. Retrieved 2008-07-22.
  51. ↑ Gena Brumitt Gruschovnik, DEBRA International Executive Committee. "DEBRA Chile website". Archived from the original on 2008-12-20. Retrieved 2008-12-19.
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