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卡尼综合征:临床与遗传学 2010 年更新。

Carney complex: Clinical and genetic 2010 update.

机构信息

Inserm U, CNRS UMR, institut Cochin, Paris, France.

出版信息

Ann Endocrinol (Paris). 2010 Dec;71(6):486-93. doi: 10.1016/j.ando.2010.08.002. Epub 2010 Sep 17.

Abstract

First described in the mid 1980s, Carney complex is a rare dominantly heritable multiple endocrine neoplasia syndrome that affects endocrine glands as the adrenal cortex, the pituitary and the thyroid. It is associated with many other nonendocrine tumors, including cardiac myxomas, testicular tumors, melanotic schwannoma, breast myxomatosis, and abnormal pigmentation or myxomas of the skin. The Carney complex gene 1 was identified 10 years ago as the regulatory subunit 1A of protein kinase A (PRKAR1A) located at 17q22-24. An inactivating heterozygous germ line mutation of PRKAR1A is observed in about two-thirds of Carney complex patients. This last decade many progresses have been done in the knowledge of this rare disease and its genetics. This review outlines the current state of this knowledge on Carney complex.

摘要

卡尼综合征于 20 世纪 80 年代中期首次被描述,是一种罕见的常染色体显性遗传性多内分泌腺肿瘤综合征,影响肾上腺皮质、垂体和甲状腺等内分泌腺。它与许多其他非内分泌肿瘤有关,包括心脏黏液瘤、睾丸肿瘤、黑色素神经鞘瘤、乳腺黏液瘤以及皮肤色素异常或黏液瘤。10 年前,卡尼综合征基因 1 被确定为蛋白激酶 A(PRKAR1A)的调节亚单位 1A(PRKAR1A),位于 17q22-24。大约三分之二的卡尼综合征患者存在 PRKAR1A 的失活杂合性 germ 系突变。在过去的十年中,人们对这种罕见疾病及其遗传学有了许多新的认识。这篇综述概述了目前对卡尼综合征的认识状况。

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