PERFORMING GONADECTOMY IN A 15-YEAR-OLD BULGARIAN GIRL WITH COMPLETE ANDROGEN INSENSITIVITY SYNDROME: A CASE REPORT

Complete Androgen Insensitivity Syndrome (CAIS) is a rare genetic Disorder of Sex Development linked to the X chromosome. It occurs due to mutations—either from mother inheritance or arising spontaneously—in the androgen receptor (AR) gene, located in the Xq11-q12 region. Individuals with CAIS have...

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Bibliografske podrobnosti

Principais autores:	Diana Hristova, Radko Tocev, Krassimir Neykov, Ibryam Ibryam, Sergei Slavov, Smail Smail
Format:	Artigo
Jezik:	Inglês
Izdano:	Peytchinski Publishing 2025-04-01
Serija:	Journal of IMAB
Teme:	complete androgen insensitivity syndrome (cais) sertoli cell adenoma hormonal replacement therapy persistence of fallopian tubes in cais
Online dostop:	https://www.journal-imab-bg.org/issues-2025/issue2/2025vol31-issue2-6143-6148.pdf
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