Hypotrichosis simplex

What is hypotrichosis simplex?

Hypotrichosis simplex is a rare form of hereditary hair loss without other abnormalities. Affected individuals typically show normal hair at birth, but experience hair loss and thinning of the hair shaft that starts during early childhood and progresses with age. Hypotrichosis simplex can be divided into 2 forms: the scalp-limited form and the generalized form, in which all body hair is affected. The progressive thinning of the hair shaft is a typical feature of androgenetic alopecia. Hypotrichosis simplex can be inherited either as an autosomal dominant or autosomal recessive trait. Some cases are caused by mutations in the APCDD1 gene on chromosome 18p11. To date, there is no treatment for this condition.

Last updated on 05-01-20

Is there treatment for hypotrichosis simplex? Is there hope for hair growth in the future?

Individuals with hypotrichosis simplex experience a gradual loss of scalp hair that begins during the middle of the first decade and results in almost complete loss of hair by the third decade. A few sparse, fine, short hairs may remain in some individuals. There is currently no treatment for hypotrichosis simplex.

Last updated on 05-01-20

Name: American Hair Loss Association 23679 Calabasas Road # 682
Calabasas, CA, 91301-1502, United States
Email: info-ahla@americanhairloss.org Url: http://americanhairloss.org

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