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Atypical aplasia cutis in association with Xia Gibbs syndrome.
Ellis, Carter; Pai, Gurpur Shashidhar; Wine Lee, Lara.
Afiliación
  • Ellis C; College of Medicine, Medical University of South Carolina, Charleston, SC, USA.
  • Pai GS; Department of Genetics, Medical University of South Carolina, Charleston, SC, USA.
  • Wine Lee L; Department of Dermatology and Dermatologic Surgery and Department of Pediatrics, Medical University of South Carolina, Charleston, SC, USA.
Pediatr Dermatol ; 38(2): 533-535, 2021 Mar.
Article en En | MEDLINE | ID: mdl-33464633
Xia Gibbs syndrome is a genetic disorder first defined in 2014 characterized by hypotonia, intellectual disability, global developmental delay, and dysmorphic facial features. While many additional features may be present, there are few reports of dermatologic findings. We report a case of atypical aplasia cutis in a female infant who was found to have Xia Gibbs syndrome. This case highlights consideration of cutaneous manifestations of Xia Gibbs syndrome which may aid in diagnosis.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Anomalías Múltiples / Displasia Ectodérmica / Discapacidad Intelectual / Anomalías Musculoesqueléticas Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Female / Humans / Infant Idioma: En Revista: Pediatr Dermatol Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Anomalías Múltiples / Displasia Ectodérmica / Discapacidad Intelectual / Anomalías Musculoesqueléticas Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Female / Humans / Infant Idioma: En Revista: Pediatr Dermatol Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos