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- Title
A novel compound heterozygous variant in the LLS gene is associated with nonsyndromic hypotrichosis.
- Authors
Morice-Picard, Fanny; Lanvin, Pierre-Louis; Lasseaux, Eulalie; Boralevi, Franck; Léauté-Labrèze, Christine; Lebreton, Louis
- Abstract
Hypotrichosis simplex is a rare form of hereditary alopecia characterized by childhood-onset sparse or absent scalp hair without structural defects. I LSS i is associated with a wide spectrum of diseases including congenital cataracts, alopecia with intellectual disability, hypotrichosis simplex and palmoplantar keratoderma-congenital alopecia syndrome type 2.
- Subjects
GENETIC variation; PALMOPLANTAR keratoderma; ALOPECIA areata; INFORMED consent (Medical law)
- Publication
Clinical & Experimental Dermatology, 2023, Vol 48, Issue 9, p1087
- ISSN
0307-6938
- Publication type
Article
- DOI
10.1093/ced/llad174