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Yonsei Medical Journal ; : 116-122, 1980.
Artigo em Inglês | WPRIM | ID: wpr-60597

RESUMO

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)


Assuntos
Adolescente , Humanos , Masculino , Bexiga Urinaria Neurogênica/etiologia , Clorotiazida/uso terapêutico , Diabetes Insípido/complicações , Diabetes Insípido/congênito , Diabetes Insípido/tratamento farmacológico , Diabetes Insípido/genética , Quimioterapia Combinada , Hidronefrose/etiologia , Indometacina/uso terapêutico
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