Autor: |
Liu, Regina, Vandiver, Amy R., Harter, Nicole, Hogeling, Marcia |
Předmět: |
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Zdroj: |
Dermatology Online Journal; 2021, Vol. 27 Issue 5, p1-4, 4p |
Abstrakt: |
We report a case of a patient with ectodermal dysplasia attributed to a heterozygous 321 C>A mutation in WNT10A who developed overlying autoimmune mediated hair loss. To the best of our knowledge this is the first reported case of alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia. This case highlights the importance of considering multiple pathways of hair loss in patients with underlying genetic defects and raises the possibility of a shared genetic predisposition. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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