斑驳病的多种表现——于里埃综合征。
Poikiloderma a varied presentation - Huriez syndrome.
作者信息
Kharge Priyadarshini, Fernendes Carol, Jairath Vijayeeta, Mohan Madan, Chandra Suresh
机构信息
Departments of Dermatology, Venereology and Leprosy, Dr. B.R Ambedkar Medical College, Bengaluru, Karnataka, India.
Department of Pathology, Dr. B.R Ambedkar Medical College, Bengaluru, Karnataka, India.
出版信息
Indian Dermatol Online J. 2015 Jan-Feb;6(1):27-30. doi: 10.4103/2229-5178.148929.
Abstract
Huriez syndrome is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma (PPK) and hypoplastic nails. We report the case of a 25 year old male, with nonfamilial Huriez syndrome.
摘要
于里埃综合征是一种罕见的常染色体显性遗传性皮肤病，其特征为远端肢体先天性硬化萎缩、掌跖角化病（PPK）和指甲发育不全三联征。我们报告一例25岁非家族性于里埃综合征男性患者。
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本文引用的文献
1
Claude Huriez and his syndrome.
Skinmed. 2011 Sep-Oct;9(5):313-4.
2
Huriez syndrome.
Indian J Dermatol Venereol Leprol. 2008 Jul-Aug;74(4):409-10. doi: 10.4103/0378-6323.42930.
3
[Spinocellular epitheliomas in congenital cutaneous atrophy in 2 families with high cancer morbidity].
Bull Soc Fr Dermatol Syphiligr. 1963 Jan-Mar;70:24-8.
4
A nonfamilial Japanese case of Huriez syndrome: p53 expression in squamous cell carcinoma.
Dermatology. 2003;207(1):82-4. doi: 10.1159/000070951.
5
Huriez syndrome: case report with a detailed analysis of skin dendritic cells.
Br J Dermatol. 2000 Nov;143(5):1091-6. doi: 10.1046/j.1365-2133.2000.03793.x.
6
An SRY-negative XX male with Huriez syndrome.
Clin Genet. 2000 Jan;57(1):61-6. doi: 10.1034/j.1399-0004.2000.570109.x.
7
A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23.
Am J Hum Genet. 2000 Jan;66(1):326-30. doi: 10.1086/302718.
8
Trends of skin cancer in the Canton of Vaud, 1976-92.
Br J Cancer. 1995 Oct;72(4):1047-53. doi: 10.1038/bjc.1995.460.
9
[Study of a probable linkage between a genodermatosis with an autosomal dominant transmission and the MNSs blood group system].
Ann Genet. 1968 Dec;11(4):217-24.
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