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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299654/ https://www.ncbi.nlm.nih.gov/pubmed/34301197 http://dx.doi.org/10.1186/s12883-021-02324-3 |