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假性甲状旁腺功能减退症

Pseudohypoparathyroidism.

作者信息

Van Dop C, Bourne H R

出版信息

Annu Rev Med. 1983;34:259-66. doi: 10.1146/annurev.me.34.020183.001355.

Abstract

Pseudohypoparathyroidism includes a genotypically diverse group of syndromes of primary resistance to hormones whose actions are mediated by cyclic adenosine 3':5'-monophosphate. In most cases, clinical presentation results from resistance to actions of parathyroid hormone, while resistance to other hormones remains subclinical. The largest subgroup of patients with this disorder, characterized by a typical somatic phenotype termed Albright's hereditary osteodystrophy, exhibits generalized deficient activity of a membrane protein that couples hormone receptors to stimulation of adenylate cyclase. Phenotypic expression of the disease varies greatly between families, within families, and even during the clinical course of individual patients. Genetic transmission occurs via several distinct loci, which produce different patterns of inheritance.

摘要

假性甲状旁腺功能减退症包括一组基因型多样的综合征,这些综合征主要表现为对由环磷酸腺苷介导其作用的激素产生抵抗。在大多数情况下,临床表现源于对甲状旁腺激素作用的抵抗,而对其他激素的抵抗仍处于亚临床状态。该疾病最大的亚组患者具有一种典型的躯体表型,称为奥尔布赖特遗传性骨营养不良,表现为将激素受体与腺苷酸环化酶刺激偶联的膜蛋白普遍活性不足。该疾病的表型表达在不同家族之间、家族内部甚至个体患者的临床病程中都有很大差异。遗传传递通过几个不同的基因座发生,这些基因座产生不同的遗传模式。

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