Φορτώνει......
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....
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Pan Afr Med J |
|---|---|
| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
The African Field Epidemiology Network
2015
|
| Θέματα: | |
| Διαθέσιμο Online: | 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 |
| Ετικέτες: |
Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!
|