Dermatological clues to the diagnosis of atypical complete DiGeorge syndrome

Academic Article


  • 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.
  • Published In

    Author List

  • Seminario-Vidal L; Kole L; Knapp C; Fort P; Kankirawatana S; Atkinson TP; McKay KM; Theos A
  • Volume

  • 22
  • Issue

  • 11