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Yonsei Medical Journal ; : 116-122, 1980.
Article in English | WPRIM | ID: wpr-60597

ABSTRACT

A 13-year-old boy was diagnosed as having primary nephrogenic diabetes insipidus, and symptoms developed at 3 years of age. Subsequently he developed bilateral hydronephrosis and a neurogenic bladder. His pedigree could be explored back 5 generations and represented an inheritance as an X-linked recessive transmission factor. He was treated with indomethacin 2 mg/kg/day plus chlorothiazide 500 mg/day and this new treatment showed a markedly decreased urine output and increased urine osmolarity. (Nephrogenic diabetes insipidus, Hydronephrosis, Indomethacin)


Subject(s)
Adolescent , Humans , Male , Urinary Bladder, Neurogenic/etiology , Chlorothiazide/therapeutic use , Diabetes Insipidus/complications , Diabetes Insipidus/congenital , Diabetes Insipidus/drug therapy , Diabetes Insipidus/genetics , Drug Therapy, Combination , Hydronephrosis/etiology , Indomethacin/therapeutic use
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