Clinical Characteristics and Management of Two Cases of Complete Androgen Insensitivity Syndrome With Germ Cell Tumors

ABSTRACT Background Androgen insensitivity syndrome (AIS) is an X‐linked recessive genetic disorder caused by mutations in the androgen receptor (AR) gene, leading to androgen resistance and disorders of sex development (DSD) in 46, XY individuals. It is classified into three phenotypes: complete (C...

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Hlavní autoři:	Fangming Wang, Dong Wang, Jianxing Li, Nianzeng Xing
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Wiley 2026-02-01
Edice:	Cancer Reports
Témata:	androgen receptor gene complete androgen‐insensitive syndrome germ cell tumors
On-line přístup:	https://doi.org/10.1002/cnr2.70491
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