Mayer-Rokitansky-Küster-Hauser Syndrome is a congenital disorder involving reproductive, genitourinary, bone, and cardiac malformations. The incidence is 1 in 4000-5000 female live births. The phenotype is female, karyotype 46 XX, with normally developed secondary sexual characteristics and functional ovaries. The occurrence of fibroids from uterine remnants in SMRKH is very rare, although a few cases have been reported in the literature. Diagnosis and approach to treatment in this case is quite complicated. Here we present a clinical case of a 30-year-old woman with SMRKH who was found to have rudimentary uterine fibroids.
| Mualliflar | Негмаджанов Баходур Болтаевич, Маматкулова Мохигул Джахангировна |
|---|---|
| Jurnal | Journal of reproductive health and uro-nephrology research (Репродуктив саломатлик ва уро-нефрологик тадқиқотлар журнали) |
| Nashr sanasi | 2023-05-20 |
| Jild | 4 |
| Son | 1 |
| Til | Rus |
синдром Майера Рокитанского-Кустера-Хаузера, миома матки, рудиментарная матка, лапароскопия, клинический случай, Mayer Rokitansky-Kuster-Hauser syndrome, uterine myoma, rudimentary uterus, laparoscopy, clinical case, Mayer Rokitanskiy-Kuster-Hauzer sindromi, bachadon miomasi, rudimentar bachadon, laparoskopiya, klinik holat
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