Shprintzen-Goldberg syndrome presenting as umbilical hernia in an Indian child

Shprintzen-Goldberg syndrome (S-G) is a rare connective tissue disorder characterised by craniosynostosis, craniofacial dysmorphism, skeletal, cardiovascular, neurological, and other abnormalities. We herein present a case of a five-year-old Indian child who presented to our clinic with reducible um...

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Detalhes bibliográficos
Main Authors: Shah, Bhushan, Sahu, Suman, Kalakoti, Piyush, Yadav, Sankalp, Syed, M M Aarif, Bhattad, Venugopal Brijmohan, Shaikh, Meena
Formato: Artigo
Idioma:Inglês
Publicado em: Australasian Medical Journal 2014
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3941576/
https://ncbi.nlm.nih.gov/pubmed/24611072
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4066/AMJ.2014.1888
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