Netherton syndrome in one Chinese adult with a novel mutation in the SPINK5 gene and immunohistochemical studies of LEKTI

Netherton syndrome in one Chinese adult with a novel mutation in the SPINK5 gene and immunohistochemical studies of LEKTI

Background : Netherton syndrome (NS) is a severe autosomal recessive ichthyosis. It is characterized by congenital ichthyosiform erythroderma, trichorrhexis invaginata, ichthyosis linearis circumflexa, atopic diathesis, and frequent bacterial infections. The disease is caused by mutations in the SPI...

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Bibliographic Details
Main Authors: Zhang Xi-Bao, Zhang San-Quan, He Yu-Qing, Luo Yu-Wu, Luo Quan, Li Chang-Xing
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2012-01-01
Series:Indian Journal of Dermatology
Subjects:
Mutation
Netherton syndrome
SPINK5 gene
Online Access:http://www.e-ijd.org/article.asp?issn=0019-5154;year=2012;volume=57;issue=4;spage=265;epage=268;aulast=Xi-Bao

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http://www.e-ijd.org/article.asp?issn=0019-5154;year=2012;volume=57;issue=4;spage=265;epage=268;aulast=Xi-Bao

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