一名女婴患先天性肾性尿崩症。
Congenital nephrogenic diabetes insipidus in a baby girl.
作者信息
Schreiner R L, Skafish P R, Anand S K, Northway J D
出版信息
Arch Dis Child. 1978 Nov;53(11):906-8. doi: 10.1136/adc.53.11.unknown.
Abstract
A 6-week-old girl with fever, hypernatraemia, dehydration, and polyuria failed to concentrate urine in response to exogenous vasopressin administration. There was no family history of nephrogenic diabetes insipidus. When she was 15 months old, the infusion of vasopressin did not produce an increase in urinary cyclic-AMP.
摘要
一名6周大的女童，伴有发热、高钠血症、脱水和多尿，对外源性血管加压素给药无尿浓缩反应。无肾性尿崩症家族史。15个月大时，血管加压素输注未使尿环磷酸腺苷增加。
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本文引用的文献
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N Engl J Med. 1969 Apr 3;280(14):750-4. doi: 10.1056/NEJM196904032801404.
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Nephrogenic diabetes insipidus and obstructive uropathy.
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Urinary cyclic adenosine monophosphate excretion in diabetes insipidus of childhood. Effect of vasopressin and chlorpropamide.
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Demonstration of a defect in the formation of adenosine 3',5'-monophosphate in vasopressin-resistant diabetes insipidus.抗血管升压素性尿崩症中3',5'-单磷酸腺苷形成缺陷的证明。
Pediatr Res. 1974 Apr;8(4):223-30. doi: 10.1203/00006450-197404000-00002.
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Cellular action of antidiuretic hormone in nephrogenic diabetes insipidus.抗利尿激素在肾性尿崩症中的细胞作用。
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