{"id":12151,"date":"2025-03-13T20:21:30","date_gmt":"2025-03-13T19:21:30","guid":{"rendered":"https:\/\/valintermed.com\/?p=12151"},"modified":"2025-03-13T20:21:30","modified_gmt":"2025-03-13T19:21:30","slug":"sindrom-mayera-rokitanskogo-kyustera-hauzera","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/sindrom-mayera-rokitanskogo-kyustera-hauzera\/","title":{"rendered":"Mayer-Rokitansky-K\u00fcster-Hauser syndrome"},"content":{"rendered":"
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Mayer-Rokitansky-K\u00fcster-Hauser syndrome (MRKH) is a genetic disorder characterized by abnormal development of the reproductive system. It primarily affects women and is characterized by the absence of the uterus and upper vaginal canal, with normal development of the ovaries and external genitalia. This syndrome is considered one of the most common conditions among reproductive system anomalies and can be associated with other anomalies, such as kidney and bone malformations. Women with MRKH syndrome usually have primary amenorrhea, although they may have normal hormone levels and sexual characteristics.<\/p>\n

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