Saudi Journal of Kidney Diseases and Transplantation · 2012 · 13 citations · 0 references
MedicineNephrologyPediatricsPediatric NephrologyRenal PathologyRenal PathophysiologyCongenital Renal AnomaliesHereditary Kidney DiseasesHereditary Renal DiseasesNeonatal Renal DisordersRenal DiseaseRenal Tubular DisordersCongenital Kidney DisordersDiabetes Insipidus SyndromesMedullary NephrocalcinosisNeonatal HydronephrosisProximal Renal Tubular AcidosisRenal DisordersRenal Metabolic DisordersRenal Tubular Dysfunction
We present a female neonate with arthrogryposis, renal tubular abnormalities and cholestasis syndrome and complex renal structural and functional abnormalities that include medullary nephrocalcinosis, hydronephrosis, nephrogenic diabetes insipidus, Fanconi syndrome, proximal and distal hyperkalemic renal tubular acidosis, near-nephrotic range proteinuria, hypercalciuria and severe hypovitaminosis D.