Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse-Sakati Syndrome: Report of a Family with Mutation in theC2orf37Gene
Author:
Affiliation:
1. As'ad Al-Hamad Dermatology Center; Al-Sabah Hospital; Kuwait City Kuwait
2. Institute of Human Genetics; University of Bonn; Bonn Germany
3. Department of Dermatology; University of Barcelona; Barcelona Spain
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/pde.12219/fullpdf
Reference15 articles.
1. A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness and ECG abnormalities;Woodhouse;J Med Genet,1983
2. Primary hypogonadism and partial alopecia in three sibs with Müllerian hypoplasia in the affected females;Al-Awadi;Am J Med Genet,1985
3. Primary hypergonadotrophic hypogonadism, partial alopecia, and Mullerian hypoplasia: report of a second family with additional findings;Mégarbané;Am J Med Genet,2003
4. Woodhouse-Sakati syndrome associated with bilateral keratoconus;Al-Swailem;Br J Ophthalmol,2006
5. Autosomal recessive syndrome with alopecia, hypogonadism, progressive extrapyramidal disorder, white matter disease, sensorineural deafness, diabetes mellitus, and low IGF1;Al-Semari;Am J Med Genet A,2007
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