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Dermatological clues to the diagnosis of atypical complete DiGeorge syndrome
Lucia Seminario-Vidal, Lauren Kole, Charles Knapp
1University of Alabama at Birmingham, Department of Dermatology, Birmingham, AL. Amy.Theos@childrensal.org.
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.
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