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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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| I publikationen: | BMC Neurol |
|---|---|
| Huvudupphovsmän: | , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2021
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| Ämnen: | |
| Länkar: | 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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