Bazex–Dupré–Christol Syndrome in a 1-Year-Old Boy and His Mother
Author:
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1470.2007.00596.x/fullpdf
Reference5 articles.
1. A case of Bazex-Dupré-Christol syndrome associated with multiple genital trichoepitheliomas
2. The Gene for Bazex-Dupré-Christol Syndrome Maps to Chromosome Xq
3. Multiple follicular hamartomas with sweat gland and sebaceous differentiation, vermiculate atrophoderma, milia, hypotrichosis, and late development of multiple basal cell carcinomas
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1. Germline intergenic duplications at Xq26.1 underlie Bazex–Dupré–Christol basal cell carcinoma susceptibility syndrome;British Journal of Dermatology;2022-12-01
2. Germline intergenic duplications at Xq26.1 underlie Bazex-Dupré-Christol syndrome, an inherited basal cell carcinoma susceptibility condition;2022-02-17
3. Importancia de las lesiones cutáneas benignas transitorias en el recién nacido y su diagnóstico diferencial;Piel;2021-08
4. Bazex-Dupré-Christol syndrome: review of clinical and molecular aspects;International Journal of Dermatology;2018-05-28
5. Disorders of Hair and Nails;Hurwitz Clinical Pediatric Dermatology;2016
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