Congenital absence of the vulva, also known as Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, is a rare congenital disorder that affects the female reproductive system. This condition primarily involves the absence or underdevelopment of the uterus and vagina, while the ovaries and external genitalia are typically unaffected.
MRKH syndrome affects approximately 1 in 5,000 female births, making it a relatively uncommon condition. The exact cause of this disorder is unknown, but it is believed to result from a combination of genetic and environmental factors during embryonic development.
Commonly diagnosed during adolescence, girls with congenital absence of the vulva typically do not experience any outward physical symptoms. However, as they reach puberty, they may notice that they do not get their period or experience difficulty with sexual intercourse due to the absence of a vaginal opening.
Diagnosis of MRKH syndrome is usually confirmed through a pelvic examination, ultrasound, and other imaging techniques. Additionally, genetic testing may be conducted to rule out other underlying genetic abnormalities.
In conclusion, congenital absence of the vulva, or Mayer-Rokitansky-Küster-Hauser syndrome, is a rare condition that affects the female reproductive system. It is crucial to raise awareness about this disorder to ensure timely diagnosis and appropriate support for affected individuals. Seeking guidance from healthcare professionals and support networks can help individuals with MRKH syndrome navigate their emotional and physical challenges.
Congenital absence of vulva, also known as Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, is a rare condition that affects the reproductive system in females. It is characterized by the absence or underdevelopment of the vulva, vagina, and uterus.
While this condition can have a significant emotional impact on those affecte...
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