Results 111 to 120 of about 5,072 (157)

Complete androgen insensitivity syndrome coexisting with müllerian duct remnants: a case report and literature review. [PDF]

Front Pediatr
Chen DL, Guo S, Chen QL, Qiu SJ, Xu YY, Zhang J, Ma HM, Li YH.   +7 more
europepmc   +1 more source

Diverse phenotypes and fertility outcomes of patients with androgen insensitivity syndrome in a Chinese family harboring identical AR gene variant. [PDF]

BMC Med Genomics
Geng H, Tang D, Li K, Xu C, Wang C, Zhang X, He X, Cao Y.   +7 more
europepmc   +1 more source

Pure 46, XY gonadal dysgenesis and 46, XY complete androgen insensitivity syndrome: A case report. [PDF]

Medicine (Baltimore)
Yu T, Liu L.
europepmc   +1 more source

A Very Early Diagnosis of Complete Androgen Insensitivity Syndrome Due to a Novel Variant in the AR Gene: A Neonatal Case Study. [PDF]

Biomedicines
Ferrante R, Tumini S, Saltarelli MA, Di Rado S, Scorrano V, Tommolini ML, Zucchelli M, Lauriola F, Lisi G, Lauriti G, Marino N, Stuppia L, Rossi C, Bucci I.   +13 more
europepmc   +1 more source

In Silico Analysis of Functional SNPs in Genes of Complete Androgen Insensitivity Syndrome (CAIS): A Retrospective, Case-Control Study. [PDF]

J Obstet Gynaecol India
Ramgir SS, Annamalai S, Abilash VG.
europepmc   +1 more source

Androgen insensitivity syndrome

The Nurse Practitioner
ABSTRACT Androgen insensitivity syndrome (AIS) is a genetic disorder impacting 46,XY individuals. It occurs in a complete form, producing a 46,XY female with female genitalia but no internal female reproductive organs; a partial form, producing a 46,XY newborn with genitalia intermediate between the classic male and female types; and ...
Singh S, Ilyayeva S.
europepmc   +4 more sources