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- W2767232806 abstract "Atypical complete DiGeorge syndrome (DGS) is an extremely rare congenital disease characterized by an eczematous dermatitis, lymphadenopathy, and an oligoclonal T-cell proliferation. Because its initial presentation may be confused with other types of eczematous dermatitis, diagnosis and treatment are usually delayed. We describe herein a case of an infant with atypical complete DGS to draw attention to the clinical and histopathological findings that lead us to the diagnosis." @default.
- W2767232806 created "2017-11-17" @default.
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- W2767232806 date "2016-01-01" @default.
- W2767232806 modified "2023-10-18" @default.
- W2767232806 title "Dermatological clues to the diagnosis of atypical complete DiGeorge syndrome" @default.
- W2767232806 doi "https://doi.org/10.5070/d32211033148" @default.
- W2767232806 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28329565" @default.
- W2767232806 hasPublicationYear "2016" @default.
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