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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Detalles Bibliográficos
Autores principales: Abidi, Kamel, Jellouli, Manel, Rabeh, Rania Ben, Hammi, Yousra, Gargah, Tahar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765342/
https://www.ncbi.nlm.nih.gov/pubmed/26958139
http://dx.doi.org/10.11604/pamj.2015.22.276.7929

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765342/
https://www.ncbi.nlm.nih.gov/pubmed/26958139
http://dx.doi.org/10.11604/pamj.2015.22.276.7929

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