Congenital uterine-vaginal aplasia or Mayer-Rokitansky-Kuester-Hauser syndrome (MRKH) is characterized by ungrown uterine buds, cervical and vaginal aplasia, but normal or hypoplastic bilateral appendages and clinically manifests as primary amenorrhea. Patients with MRKH have a normal female phenotype and karyotype development (46, XX) and an incidence of 1 per 4,000 or 5,000 newborns
| Mualliflar | Адылова М.Н, Негмаджанов Б.Б, Раббимова Г.Т |
|---|---|
| Jurnal | Journal of reproductive health and uro-nephrology research (Репродуктив саломатлик ва уро-нефрологик тадқиқотлар журнали) |
| Nashr sanasi | 2022-10-27 |
| Jild | 3 |
| Son | 3 |
| Til | Rus |
маточно–вагинальная аплазия, аплазия Майера-Рокитанского-Синдром-Кюстера-Хаузера, гипопластическим двусторонним придатком, первичная аменорея, uterovaginal aplasia, Mayer-Rokitansky-Kuester-Hauser syndrome, hypoplastic bilateral appendage, primary amenorrhea, utero-vaginal aplaziya, Mayer-Rokitanskiy aplaziyasi-sindromi, gipoplastik ikki tomonlama bachadon ortiqlari, birlamchi amenoreya
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Aplasia of the uterus and vagina are among the most common anomalies in the development of female genital organs characterized by a variety of forms of clinical symptoms and high percentage of diagnostic and treatment…
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