Atypical aplasia cutis in association with Xia Gibbs syndrome.
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.
Palabras clave
Texto completo:
1
Bases de datos:
MEDLINE
Asunto principal:
Anomalías Múltiples
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Displasia Ectodérmica
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Discapacidad Intelectual
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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