Hereditary renal tubular disorders in Turkey: demographic, clinical, and laboratory features
CLINICAL AND EXPERIMENTAL NEPHROLOGY, vol.15, no.1, pp.108-113, 2011 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 15 Issue: 1
- Publication Date: 2011
- Doi Number: 10.1007/s10157-010-0367-z
- Journal Name: CLINICAL AND EXPERIMENTAL NEPHROLOGY
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Page Numbers: pp.108-113
- Keywords: Bartter's syndrome, Cystinosis, Demography, dRTA, Failure to thrive, Features, Gitelman's syndrome, Hereditary renal tubular disorders, Prevalence, pRTA, ACIDOSIS, MUTATIONS, DEAFNESS
- Akdeniz University Affiliated: Yes
Abstract
The Turkish Renal Tubular Disorders Working Group aimed to form a patient registry database and gathered demographic, clinical, and laboratory data in various hereditary renal tubular disorders (HRTDs).