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A Novel Mutation of PRKAR1A Caused Carney Complex in a Chinese Patient 被引量:1

A Novel Mutation of PRKAR1A Caused Carney Complex in a Chinese Patient
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摘要 Primary pigmented nodular adrenocortical disease (PPNAD) causes adrenocorticotropic hormone (ACTH)-independent Cushing's syndrome (CS),which is the most frequent endocrine manifestation of Carney complex (CNC).[1] In the disease process of PPNAD,both presadrenal glands are involved and feature small brown-black nodules separated by the atrophic adrenal cortex. Primary pigmented nodular adrenocortical disease (PPNAD) causes adrenocorticotropic hormone (ACTH)-independent Cushing's syndrome (CS),which is the most frequent endocrine manifestation of Carney complex (CNC).[1] In the disease process of PPNAD,both presadrenal glands are involved and feature small brown-black nodules separated by the atrophic adrenal cortex.
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2017年第24期3009-3010,共2页 中华医学杂志(英文版)
关键词 Carney Complex CHINESE MUTATION PRKAR1A Gene Carney Complex Chinese Mutation PRKAR1A Gene
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