A Rare Syndrome Resembling Scleroderma: Huriez Syndrome
Author:
Publisher
S. Karger AG
Subject
Dermatology
Reference5 articles.
1. Sekar SC, Srinivas CR: Huriez syndrome. Indian J Dermatol Venereol Leprol 2008;74:409-410.
2. Watanabe E, Takai T, Ichihashi M, Ueda M: A nonfamilial Japanese case of Huriez syndrome: P53 expression in squamous cell carcinoma. Dermatology 2003;207:82-84.
3. Vernole P, Terrinoni A, Didona B, De Laurenzi V, Rossi P, Melino G, et al: An SRY-negative XX male with Huriez syndrome. Clin Genet 2000;57:61-66.
4. Levi F, Franceschi S, Te VC, Randimbison L, La Vecchia C: Trends of skin cancer in the Canton of Vaud, 1976-92. Br J Cancer 1995;72:1047-1053.
5. Lee, Young-Ae, et al: A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23. Am J Hum Genet 2000;66:326-330.
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1. Scleroderma and scleroderma-like syndromes;Frontiers in Immunology;2024-06-03
2. Immunologic and nonimmunologic sclerodermal skin conditions - review;Frontiers in Immunology;2023-07-12
3. Overview of familial syndromes with increased skin malignancies;Archives of Dermatological Research;2022-11-07
4. Huriez syndrome: Additional pathogenic variants supporting allelism to SMARCAD syndrome;American Journal of Medical Genetics Part A;2022-02-25
5. Clinical and Histopathological Features of Scleroderma-like Disorders: An Update;Medicina;2021-11-20
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