换一批
换一批Clinical Features of an Unrecognized 21-hydroxylase Deficiency Woman During Controlled Ovarian Hyperstimulation
摘要To the Editor:Nonclassic congenital adrenal hyperplasia (NCAH) due to 21-hydroxylase deficiency (21-OHD) is one of the most common autosomal recessive disorders.Affected individuals typically present signs and symptoms related to excessive androgens.[1] In the process of assisted reproductive technique (ART),the clinical features of NCAH may evade our attention and,therefore,be left untreated.Here,we present a case of NCAH,who underwent controlled ovarian hyperstimulation (COH).
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栏目名称
Correspondence
DOI
10.4103/0366-6999.163378
发布时间
2015-09-24
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