Article
Autosomal recessive hyper-IgE syndrome caused by DOCK8 gene mutation with new clinical features: a case report.
BMC neurology - 23 Jul 2021
Yang Jing, Liu Yan
Abstract excerpt
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 with a new clinic features caused by DOCK8 gene mutations. CASE PRESENTATION: A 7-year-old girl was admitted to our...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
