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  2. Müllerian agenesis - Wikipedia

    en.wikipedia.org/wiki/Müllerian_agenesis

    Müllerian agenesis (including absence of the uterus, cervix and/or vagina) is the cause in 15% of cases of primary amenorrhoea. [2] Because most of the vagina does not develop from the Müllerian duct, instead developing from the urogenital sinus, along with the bladder and urethra, it is present even when the Müllerian duct is completely absent.

  3. Müllerian anomalies - Wikipedia

    en.wikipedia.org/wiki/Müllerian_anomalies

    The prevalence of vaginal agenesis or class I uterine anomalies is 1:5000 female live births globally. The most prevalent form of vaginal agenesis is Mayer–Rokitansky–Kuster–Hauser (MRKH) syndrome and results in congenital aplasia or hypoplasia of Müllerian derived structures. [9] MRKH syndrome account for 5% to 10% of all Müllerian ...

  4. Paramesonephric duct - Wikipedia

    en.wikipedia.org/wiki/Paramesonephric_duct

    The paramesonephric ducts play a critical role in the female reproductive tract and differentiate to form the uterine tubes, uterus, superior vagina as well as the uterine cervix. Many types of disorders can occur when this system is disrupted ranging from uterine and vaginal agenesis to the duplication of unwanted cells of the uterus and vagina.

  5. What Is Pelvic Floor Dysfunction in Men? Causes, Symptoms ...

    www.aol.com/lifestyle/pelvic-floor-dysfunction...

    The causes of pelvic floor dysfunction aren’t well understood. Experts know that weakened muscles and connective tissue in the pelvis can contribute to it, as can injuries to the pelvis.

  6. Persistent Müllerian duct syndrome - Wikipedia

    en.wikipedia.org/wiki/Persistent_Müllerian_duct...

    The genetic mutational cause of PMDS, is a 27 base-pair deletion of the Anti-Müllerian Type 2 Receptor gene. The 27-base-pair deletion that occurs PMDS is in exon 10 on one allele. [ 9 ] With the AMHR2 gene mutation (PMDS Type 2), the AMHR2 is either not produced, produced in deficient amounts, defective, or the Müllerian ducts manifested a ...

  7. Kallmann syndrome - Wikipedia

    en.wikipedia.org/wiki/Kallmann_syndrome

    [8] [3] Between 35 and 45% of cases of KS/CHH have an unknown genetic cause. [28] The ANOS1 gene defect (previously known as KAL-1) was the first one discovered and the one most commonly tested for. It causes the x-linked form of Kallmann syndrome and is associated with the additional symptoms of anosmia, bimanual synkinesis and renal agenesis ...