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

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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Bibliographic Details
Main Authors: Jing Yang, Yan Liu
Format: Article
Language:English
Published: BMC 2021-07-01
Series:BMC Neurology
Subjects:
Hyper IgE syndrome
DOCK8 gene mutation
Facial paralysis
New clinic features
Online Access:https://doi.org/10.1186/s12883-021-02324-3

Internet

https://doi.org/10.1186/s12883-021-02324-3

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