Uterus Didelphys

Uterus didelphys is a rare congenital uterine anomaly where a female is born with two separate uteri, each connected to a cervix and possibly a double vagina. This condition occurs during fetal development when the Müllerian ducts fail to fuse properly.

Cause

The exact cause of uterus didelphys is not well understood, but it is believed to be related to genetic mutations or environmental factors that affect the development of the reproductive system during embryogenesis. The condition is usually diagnosed incidentally during pelvic examination, imaging studies, or surgery for other indications.

Symptoms

Women with uterus didelphys may experience a range of symptoms, including:

Diagnosis

The diagnosis of uterus didelphys is typically made using a combination of imaging studies and physical examination. The following tests may be used:

Treatment

The treatment for uterus didelphys depends on the individual's symptoms, fertility goals, and overall health. The following options may be considered:

  • No treatment: if the condition is asymptomatic and does not affect fertility or menstrual function
  • Surgical correction: to remove any obstructive tissue, repair vaginal septa, or unify the uteri
  • Hormonal therapy: to regulate menstrual cycles and reduce symptoms
  • Assisted reproductive technology (ART): to improve fertility outcomes in women with uterus didelphys

Complications

Women with uterus didelphys are at increased risk for several complications, including:

  • Infertility or recurrent miscarriages
  • Pregnancy complications, such as preterm labor or fetal growth restriction
  • Urinary tract infections or other urinary symptoms due to the abnormal anatomy
  • Endometriosis or other gynecologic conditions

Prognosis

The prognosis for women with uterus didelphys varies depending on the severity of the condition, fertility goals, and overall health. With proper diagnosis and treatment, many women with uterus didelphys can experience significant improvement in symptoms and quality of life.

Frequently Asked Questions (FAQs)

What is Uterus Didelphys?
A rare congenital condition where a woman has two uteruses.

What causes Uterus Didelphys?
Abnormal development of the Müllerian ducts during fetal development.

How common is Uterus Didelphys?
Occurs in about 1 in 2,000 to 1 in 3,000 female births.

What are the symptoms of Uterus Didelphys?
Often asymptomatic, but can include pelvic pain, heavy menstrual bleeding, and infertility.

Can women with Uterus Didelphys get pregnant?
Yes, but may have higher risk of miscarriage, preterm labor, and ectopic pregnancy.

How is Uterus Didelphys diagnosed?
Typically through ultrasound, MRI, or laparoscopy.

Is treatment necessary for Uterus Didelphys?
Not always, but surgery may be recommended to correct related anatomical issues.

Can Uterus Didelphys increase the risk of other health problems?
May increase risk of endometriosis, cervical abnormalities, and kidney problems.

Is Uterus Didelphys inherited?
No, it is a congenital condition that occurs during fetal development.

Can women with Uterus Didelphys have a normal pregnancy and delivery?
Yes, but may require closer monitoring and special care during pregnancy.

Article last updated on: 25th June 2025.
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