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

Abstract 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...

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Autors principals:	Jing Yang, Yan Liu
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2021-07-01
Col·lecció:	BMC Neurology
Matèries:	Hyper IgE syndrome DOCK8 gene mutation Facial paralysis New clinic features
Accés en línia:	https://doi.org/10.1186/s12883-021-02324-3
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