These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Atypical aplasia cutis in association with Xia Gibbs syndrome.
    Author: Ellis C, Pai GS, Wine Lee L.
    Journal: Pediatr Dermatol; 2021 Mar; 38(2):533-535. PubMed ID: 33464633.
    Abstract:
    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] [Full Text] [Related] [New Search]