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....

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Pan Afr Med J
Asıl Yazarlar: Abidi, Kamel, Jellouli, Manel, Rabeh, Rania Ben, Hammi, Yousra, Gargah, Tahar
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The African Field Epidemiology Network 2015
Konular:
Case Report
Online Erişim: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
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller