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Due to a very broad range of anomalies it is very difficult to diagnose paramesonephric duct anomalies. [9] Due to improved surgical instruments and technique, women with paramesonephric duct anomalies can have normal sexual relations. Through the use of Vecchietti and Mclndoe procedures, women can carry out their sexual activity. [9]
Müllerian duct anomalies are those structural anomalies caused by errors in Müllerian duct development as an embryo forms. Factors contributing to them include genetics and maternal exposure to substances that interfere with fetal development. [1] [2] Genetic causes of Müllerian duct anomalies are complicated and uncommon.
Müllerian agenesis, also known as Müllerian aplasia, vaginal agenesis, or Mayer–Rokitansky–Küster–Hauser syndrome (MRKH syndrome), is a congenital malformation characterized by a failure of the Müllerian ducts to develop, resulting in a missing uterus and variable degrees of vaginal hypoplasia of its upper portion.
Women with the condition may be asymptomatic and unaware of having a unicornuate uterus; normal pregnancy may occur. In a review of the literature Reichman et al. analyzed the data on pregnancy outcome of 290 women with a unicornuate uterus. 175 women had conceived for a total of 468 pregnancies.
A uterine malformation is a type of female genital malformation resulting from an abnormal development of the Müllerian duct(s) during embryogenesis. Symptoms range from amenorrhea, infertility, recurrent pregnancy loss, and pain, to normal functioning depending on the nature of the defect.
Ciliated cyst of the vulva, also known as cutaneous Müllerian cyst and paramesonephric mucinous cyst of the vulva, is a cutaneous condition characterized by a cyst of the vulva. [ 1 ] See also
Historically, the cause of nasopalatine duct cysts has been somewhat of an enigma. Although it was originally postulated that the cyst formed from trapped epithelial cells during embryonic fusion of the palatal bones, [3] it is now thought that it forms from oronasal ducts present within the incisive canals. [4] [5]
There is a small association between Gartner's duct cysts and metanephric urinary anomalies, such as ectopic ureter and ipsilateral renal hypoplasia. [5] Symptoms of a Gartner's duct cyst include: infections, bladder dysfunction, abdominal pain, vaginal discharge, and urinary incontinence. [6] The size of the cyst is usually less than 2 cm.