Netherton syndrome previously misdiagnosed as hyper IgE syndrome caused by a probable mutation in SPINK5 C

Netherton syndrome (NS, MIM256500) is an autosomal recessive disorder that includes ichthyosis linearis circumflexa and a predisposition to allergies, asthma, and eczema, with hypereosinophilia, trichorrhexis invaginata, and elevated serum IgE levels. The genetic bases of Netherton syndrome are mut...

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書目詳細資料
發表在:The Turkish Journal of Pediatrics
Main Authors: Kemal Özyurt, Mustafa Atasoy, Ragıp Ertaş, Yılmaz Ulaş, Muhammed Reşat Akkuş, Aslıhan Kiraz, Hans Christian Hennies
格式: Article
語言:英语
出版: Hacettepe University Institute of Child Health 2019-08-01
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在線閱讀:https://turkjpediatr.org/article/view/742