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11β-羟化酶缺乏所致先天性肾上腺皮质增生症中的盐丢失。

Salt loss in congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.

作者信息

Hochberg Z, Benderly A, Zadik Z

出版信息

Arch Dis Child. 1984 Nov;59(11):1092-4. doi: 10.1136/adc.59.11.1092.

Abstract

Nine patients with 11 beta-hydroxylase deficiency had 13 episodes of gastroenteritis requiring hospital admission and fluid administration. Eight episodes were accompanied by hyponatraemia and salt loss. The salt losing patients were treated with excessive glucocorticoid and those with normal serum sodium concentrations were treated with inadequate glucocorticoid. Excessive glucocorticoid suppressed deoxycorticosteroid secretion, resulting in salt loss.

摘要

9例11β-羟化酶缺乏患者发生13次需住院及补液治疗的肠胃炎发作。8次发作伴有低钠血症和失盐。失盐患者接受了过量糖皮质激素治疗,而血清钠浓度正常的患者接受了不足量的糖皮质激素治疗。过量糖皮质激素抑制脱氧皮质酮分泌,导致失盐。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e19b/1628810/a962b7727a9d/archdisch00728-0096-a.jpg

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