Short anagen syndrome

Last updated
Short anagen syndrome
Specialty Dermatology

Short anagen syndrome is a condition where hair does not grow beyond a short length, due to an unusually short duration of active hair growth (anagen phase). [1] Most cases are associated with fine blond hair. [2]

Contents

Signs and symptoms

Short anagen syndrome appears as sporadic short hair, frequently with low hair density and no obvious alopecia patches. [3] Oftentimes, parents worry that their child never needs a haircut or that their hair never gets long. [4] The anagen phase lasts for only four to ten months. [5] The hair cycle synchronizes when the anagen phase shortens, resulting in recurrent periods of severe hair loss. [1]

Causes

Although familial cases have been described, which may indicate an autosomal dominant inheritance, [6] the condition is congenital and is believed to be sporadic. [1]

Diagnosis

As of right now, short anagen syndrome lacks diagnostic standards. Nonetheless, the diagnosis might be supported by the following six key clinical features: [4]

  1. Other than its length, the hair shaft is normal. [4]
  2. Normal hair density. [4]
  3. Absence of fragility in hair. [4]
  4. When separating it from loose anagen syndrome or telogen effluvium, the hair pull test is frequently normal. [4]
  5. Normal physical exam (skin, teeth, and nails). [4]
  6. Average physical and mental growth. [4]

The diagnosis is confirmed by microscopic analysis of the hair, which displays short telogen hairs with tapering tips, indicating uncut hairs. [1]

Differential diagnosis for short hair consists primarily of loose anagen syndrome (LAS), congenital hypotrichosis, and hair shaft diseases. [5]

Treatment

Topical minoxidil is known to prolong the anagen phase, enhance hair length, and prevent telogen effluvium as a therapeutic intervention; nevertheless, therapy is debatable and may not be required, at least in young children. [7] [8]

See also

Related Research Articles

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

Alopecia areata, also known as spot baldness, is a condition in which hair is lost from some or all areas of the body. It often results in a few bald spots on the scalp, each about the size of a coin. Psychological stress and illness are possible factors in bringing on alopecia areata in individuals at risk, but in most cases there is no obvious trigger. People are generally otherwise healthy. In a few cases, all the hair on the scalp is lost, or all body hair is lost. Hair loss can be permanent, or temporary.

<span class="mw-page-title-main">Hair loss</span> Loss of hair from the head or body

Hair loss, also known as alopecia or baldness, refers to a loss of hair from part of the head or body. Typically at least the head is involved. The severity of hair loss can vary from a small area to the entire body. Inflammation or scarring is not usually present. Hair loss in some people causes psychological distress.

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

Telogen effluvium is a scalp disorder characterized by the thinning or shedding of hair resulting from the early entry of hair in the telogen phase. It is in this phase that telogen hairs begin to shed at an increased rate, where normally the approximate rate of hair loss is 125 hairs per day.

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

Pili torti is characterized by short and brittle hairs that appear flattened and twisted when viewed through a microscope.

Anagen effluvium is the pathologic loss of anagen or growth-phase hairs. Classically, it is caused by radiation therapy to the head and systemic chemotherapy, especially with alkylating agents.

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

Loose anagen syndrome, also known as loose anagen hair syndrome, is a hair disorder related to dermatology. It is characterised by the easy and pain free detachment of anagen staged hairs from the scalp. This hair condition can be spontaneous or genetically inherited.

<span class="mw-page-title-main">Acrokeratoelastoidosis of Costa</span> Medical condition

Acrokeratoelastoidosis of Costa or Acrokeratoelastoidosis is a hereditary form of marginal keratoderma, and can be defined as a palmoplantar keratoderma. It is distinguished by tiny, firm pearly or warty papules on the sides of the hands and, occasionally, the feet. It is less common than the hereditary type of marginal keratoderma, keratoelastoidosis marginalis.

Pressure alopecia, also known as postoperative alopecia, and pressure-induced alopecia, occurs in adults after prolonged pressure on the scalp during general anesthesia, with the head fixed in one position, and may also occur in chronically ill persons after prolonged bed rest in one position that causes persistent pressure on one part of the scalp, all likely due to pressure-induced ischemia.

Spotted lunulae is a distinctive change that occurs with alopecia areata.

Melanonychia is a black or brown pigmentation of a nail, and may be present as a normal finding on many digits in Afro-Caribbeans, as a result of trauma, systemic disease, or medications, or as a postinflammatory event from such localized events as lichen planus or fixed drug eruption.

Pili bifurcati is characterized by bifurcation found in short segments along the shafts of several hairs, with each branch of the bifurcation being covered with its own cuticle.

Pili annulati is a genetic trait in which the hair seems 'banded' by alternating segments of light and dark color when seen in reflected light.

Non scarring hair loss, also known as noncicatricial alopecia is the loss of hair without any scarring being present. There is typically little inflammation and irritation, but hair loss is significant. This is in contrast to scarring hair loss during which hair follicles are replaced with scar tissue as a result of inflammation. Hair loss may be spread throughout the scalp (diffuse) or at certain spots (focal). The loss may be sudden or gradual with accompanying stress.

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

Trichoscopy is a method of hair and scalp evaluation and is used for diagnosing hair and scalp diseases. The method is based on dermoscopy. In trichoscopy hair and scalp structures may be visualized at many-fold magnification. Currently magnifications ranging from 10-fold to 70-fold are most popular in research and clinical practice.

Malalignment of the nail plate, also known as congenital malalignment of the great toenails or congenital malalignment syndrome, is a congenital malalignment of the nail of the great toe, and is often misdiagnosed although it is a common condition. It most commonly affects the hallucices. The nail might be discolored and develop infections. If the misaligned nail becomes embedded in the lateral nail fold it can cause pain, inflammation and erythema.

An eccrine nevus is an extremely rare cutaneous condition that, histologically, is characterized by an increase in size or number of eccrine secretory coils. Hyperhidrosis is the most common symptom. It can present as discoloured nodules, papules, or plaques. Eccrine nevus mostly affects the extremities. Eccrine nevus are diagnosed based of histology. Treatment includes surgical excision or topical medications.

Idiopathic facial aseptic granuloma is a cutaneous condition characterized by a chronic, painless, solitary nodule, reminiscent of an acne nodule, appearing on the cheeks of young children. It has a prolonged course, but spontaneously heals.

Rheumatoid neutrophilic dermatitis, also known as rheumatoid neutrophilic dermatosis, is a cutaneous condition associated with rheumatoid arthritis.

Congenital erosive and vesicular dermatosis is a cutaneous condition characterized by generalized erosions, vesicles, crusting and ‘scalded skin-like’ erythematous areas affecting up to 75% of the body surface area.

<span class="mw-page-title-main">Absence of fingerprints-congenital milia syndrome</span> Medical condition

Absence of fingerprints-congenital milia syndrome, also known simply as Baird syndrome is an extremely rare autosomal dominant genetic disorder which is characterized by a lack of fingerprints and the appearance of blisters and facial milia soon after birth. It has been described in ten families worldwide.

References

  1. 1 2 3 4 Giacomini, Federica; Starace, Michela; Tosti, Antonella (2011). "Short Anagen Syndrome". Pediatric Dermatology. 28 (2). Wiley: 133–134. doi:10.1111/j.1525-1470.2010.01165.x. ISSN   0736-8046. PMID   20553398.
  2. Avashia, N; Woolery-Lloyd H; Tosti A; Romanelli P (December 2010). "Short anagen syndrome in an African American woman". Journal of the American Academy of Dermatology. 63 (6): 1092–3. doi:10.1016/j.jaad.2009.10.019. PMID   20546972.
  3. Antaya, Richard J.; Sideridou, Eirini; Olsen, Elise A. (2005). "Short anagen syndrome". Journal of the American Academy of Dermatology. 53 (2). Elsevier BV: S130–S134. doi:10.1016/j.jaad.2004.12.029. ISSN   0190-9622.
  4. 1 2 3 4 5 6 7 8 Yisheng, Wong; Peiqi, Su (August 2023). "Short Anagen Syndrome: A Hair Cycle Disorder Not To Be Forgotten". Asian Journal of Pediatric Dermatology. 1 (1): 24. doi: 10.4103/3333-8888.384062 (inactive 2024-05-11). ISSN   2950-3515.{{cite journal}}: CS1 maint: DOI inactive as of May 2024 (link)
  5. 1 2 Oberlin, Kate E.; Maddy, Austin J.; Martínez-Velasco, María Abril; Vázquez-Herrera, Norma Elizabeth; Schachner, Lawrence A.; Tosti, Antonella (2018). "Short anagen syndrome: Case series and literature review". Pediatric Dermatology. 35 (3): 388–391. doi:10.1111/pde.13478. ISSN   0736-8046. PMID   29582461.
  6. Barraud-Klenovsek, M.M.; Trüeb, R.M. (2000). "Congenital hypotrichosis due to short anagen". British Journal of Dermatology. 143 (3). Oxford University Press (OUP): 612–617. doi:10.1111/j.1365-2133.2000.03720.x. ISSN   0007-0963. PMID   10971339.
  7. Cheng, Yu‐Pin; Chen, Yu‐Sheng; Lin, Sung‐Jan; Hsiao, Cheng‐Hsiang; Chiu, Hsien‐Ching; Chan, Jung‐Yi Lisa (2016-10-05). "Minoxidil improved hair density in an Asian girl with short anagen syndrome: a case report and review of literature". International Journal of Dermatology. 55 (11). Wiley: 1268–1271. doi:10.1111/ijd.12150. ISSN   0011-9059.
  8. JUNG, Hee Dam; KIM, Jung Eun; KANG, Hoon (2011-05-04). "Short anagen syndrome successfully controlled with topical minoxidil and systemic cyclosporine A combination therapy". The Journal of Dermatology. 38 (11). Wiley: 1108–1110. doi:10.1111/j.1346-8138.2011.01222.x. ISSN   0385-2407.

Further reading