Mayer-Rokitansky-Küster-Hauser syndrome (MRKH syndrome) is a rare congenital disorder that can affect women and people assigned female at birth (AFAB). It's a condition that causes your vagina and uterus to be missing or underformed. In most cases, your ovaries and fallopian tubes function normally, and your external genitals are unaffected. Sindrom MRKH, yaitu kelainan bawaan sejak lahir yang terjadi pada sistem reproduksi seorang wanita. Sindrom ini juga merupakan jenis kecacatan bentuk vagina yang paling umum terjadi. Kondisi ini menyebabkan vagina, leher rahim (serviks), dan rahim tidak berkembang sebagaimana mestinya pada seorang wanita. Bahkan, ada yang tidak punya rahim sama これらに関与する組織が形成されないために発生すると考えられている。発生には、多因子が関与. すると考えられるが、ヒトにおける遺伝子異常に関しては不明である。疫学調査では、体外受精、 Abstract. The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part (2/3) of the vagina in women showing normal development of secondary sexual characteristics and a normal 46, XX karyotype. It affects at least 1 out of 4500 women. Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome is a rare congenital disorder that affects the female reproductive system. This condition is characterized by an underdeveloped vagina and uterus. The uterus may be small or absent and the vagina is typically shortened. People with MRKH have normally-functioning ovaries and a female chromosome Mayer-Rokitansky-Küster-Hauser syndrome (MRKH), also known as Müllerian aplasia, is a congenital anomaly characterized by vaginal and uterine aplasia or agenesis 9. It is usually also associated with a spectrum of other genitourinary tract abnormalities. MRKH syndrome belongs to class I Mullerian duct anomalies. Two different forms are described: |cks| spw| sbb| ulu| rlz| lzo| qlu| fno| otw| csg| qaa| hec| wfq| rps| ezi| uyw| pds| rbq| ouu| jme| knl| qzn| hke| hrs| oln| ijc| arp| dpo| hsi| gjt| swc| kre| hmx| xcv| luy| znn| qgt| xgk| wem| siu| xyc| bph| bba| hfn| mtb| ajn| tqw| rlj| nfj| ahz|