Research advances of Netherton syndrome

Research advances of Netherton syndrome

Netherton syndrome (NS) is a rare recessive syndromic ichthyosis due to mutations in the SPINK5 gene characterized by a triad of congenital ichthyosiform erythroderma (CIE) and/or ichthyosis linearis circumflexa (ILC), hair shaft abnormalities, and elevated IgE levels. However, NS patients often suf...

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Bibliographic Details
Main Authors: Xiaoxuan CHEN, Guiyue CAI, Ruitao ZOU, Rongyi CHEN
Format: Article
Language:zho
Published: editoiral office of Journal of Diagnosis and Therapy on Dermato-venereology 2022-04-01
Series:Pifu-xingbing zhenliaoxue zazhi
Subjects:
netherton syndrome
spink5 gene
pathogenesis progression
treatment advancement
Online Access:http://pfxbzlx.gdvdc.com/CN/10.3969/j.issn.1674-8468.2022.02.020

Internet

http://pfxbzlx.gdvdc.com/CN/10.3969/j.issn.1674-8468.2022.02.020

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