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Aisyatul Mukminah
Laboratorium / SMF Obstetri dan Ginekologi FK Unibraw
Medicine & Pharmacology

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PENATALAKSANAAN SINDROMA MAYER ROKITANSKY KUSTER HAUSER (SINDROMA MRKH) DENGAN SINDROMA KLIPPEL FEIL Wiyasa IW, Arsana; Mukminah, Aisyatul
Jurnal Kedokteran Brawijaya Vol 20, No 2 (2004)
Publisher : Fakultas Kedokteran Universitas Brawijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (106.457 KB) | DOI: 10.21776/ub.jkb.2004.020.02.7

Abstract

ABSTRACT It was reported that a 19 year old woman, suffered from Muller duct agenesis. The patient came to RSSA, complained about primary amenorrhea and assimetrical of head position. Tuba, uterus and 2/3 proximal vagina were not formed. Both of ovaries seemed normal. Based on vaginal sondage, the vagina canal is only 1.5 cm. Secondary sexual characteristics developed normally. By skull and cervical X – ray, it was found fusion of vertebrae cervical 3, 4. The vagina and the uterus are not present, but the tuba and the ovarium are normal; this case is known as Mayer Rokitansky Kuster Hauser Syndrome. Moreover, it is accompanied by another congenital defect, i.e. fusion of vertebrae cervical 3 and 4, which is called Klippel Feil Syndrome. In the exploration, it was found that there was a constitution of cromosom 46,XX. It has been done hormonal examination: FSH, LH, estrogen, prolactin and was obtained testosteron < 127.8 ng/dl. The patient was grews up as a woman. Her behavior, attitude, emotion and sexual behavior are likely a woman.  We plan to perform and suggest her to adopts a child. To treat the Klippel Feil, it is important prevention of the neck trauma and complication of neurology and arthritis. Key word : Mayer Rokitansky Kuster Hauster Syndrome, Klippel Feil Syndrome, vaginoplasty
Co-Authors Arsana Wiyasa IW