A Case of Bilateral Testicular Tumors Subsequently Diagnosed as Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

A Case of Bilateral Testicular Tumors Subsequently Diagnosed as Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

21-hydroxylase deficiency (21-OHD) caused congenital adrenal hyperplasia (CAH) is a group of autosomal recessive genetic disorders resulting from mutations in genes involved with cortisol (CO) synthesis in the adrenal glands. Testicular adrenal rest tumors (TARTs) are rarely the presenting symptoms...

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Bibliographic Details
Main Authors: Yan-Kun Sha, Yan-Wei Sha, Lu Ding, Wei-Wu Liu, Yue-Qiang Song, Jin Lin, Xue-Mei He, Ping-Ping Qiu, Ling Zhang, Ping Li
Format: Article
Language:English
Published: Royan Institute (ACECR), Tehran 2016-01-01
Series:International Journal of Fertility and Sterility
Subjects:
21
hydroxylase deficiency
congenital adrenal hyperplasia
precocious puberty
Online Access:http://www.ijfs.ir/article_45351_2ae9cdfab26e2d6ab354a12ef1209b44.pdf

Internet

http://www.ijfs.ir/article_45351_2ae9cdfab26e2d6ab354a12ef1209b44.pdf

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