Williams-Beuren syndrome associated with single kidney and nephrocalcinosis: a case report

Williams-Beuren syndrome is a rare neurodevelopmental disorder, characterized by congenital heart defects, abnormal facial features, mental retardation with specific cognitive and behavioral profile, growth hormone deficiency, renal and skeletal anomalies, inguinal hernia, infantile hypercalcaemia....

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Bibliografiske detaljer
Udgivet i:Pan Afr Med J
Main Authors: Abidi, Kamel, Jellouli, Manel, Rabeh, Rania Ben, Hammi, Yousra, Gargah, Tahar
Format: Artigo
Sprog:Inglês
Udgivet: The African Field Epidemiology Network 2015
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4765342/
https://ncbi.nlm.nih.gov/pubmed/26958139
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2015.22.276.7929
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