Autor:	Ellis, Carter, Pai, Gurpur Shashidhar, Wine Lee, Lara
Předmět:	GENETIC disorders SYNDROMES INFANTS DEVELOPMENTAL delay CUTANEOUS manifestations of general diseases OCULAR hypotony
Zdroj:	Pediatric Dermatology; Mar2021, Vol. 38 Issue 2, p533-535, 3p
Abstrakt:	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. [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
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