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Autosomal recessive hyper-IgE syndrome caused by DOCK8 gene mutation with new clinical features: a case report

BACKGROUND: Autosomal recessive hyper-IgE syndrome (AR-HIES) caused by DOCK8 gene is a rare immunodeficiency disease, the main clinical manifestations include recurrent Eczema-like rash, skin and lung abscesses, accompanied with increased serum IgE level. Here, we report a 7-year-old Chinese girl wi...

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Библиографические подробности
Опубликовано в: :BMC Neurol
Главные авторы: Yang, Jing, Liu, Yan
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2021
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC8299654/
https://ncbi.nlm.nih.gov/pubmed/34301197
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-021-02324-3
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