Uterine anomalies medically termed as Mullerian anomalies are congenital structural irregularities in the uterus that alter its shape, size, or structure. These abnormalities may impact menstrual health, fertility, and pregnancy outcomes.
Common Uterine Malformations and Treatment
Girls with Müllerian anomalies may exhibit symptoms such as:
Surgical interventions are often performed to:
Advanced imaging techniques play a crucial role in identifying uterine anomalies:
Treatment approaches are tailored to the specific type of anomaly and may include:
At Life Plus Hospital, we offer:
Professionals having extensive training in identifying uterine abnormalities and carrying out surgical repairs.
Using minimally invasive techniques guarantees better outcomes and a speedier recovery.
We assist patients throughout their diagnosis and recuperation.
Since each case is different, we adjust our strategy to suit each client's requirements.
If you suspect or have been diagnosed with a uterine anomaly and experience symptoms like pelvic pain or recurrent miscarriages, LifePlus Hospital is here to support you. Schedule a consultation today to learn how fertility and uterine anomaly repair can improve your health and quality of life.
Müllerian anomalies are rare, affecting approximately 1 in 4,000 to 5,000 women. However, some mild forms may go undiagnosed due to minimal symptoms or detection only during investigations for infertility or other reproductive issues.
Yes, Müllerian anomalies can affect fertility. Depending on the type and severity of the anomaly, they may interfere with the implantation of an embryo or cause miscarriage. Some anomalies, such as a septate uterus, can be surgically corrected to improve the chances of pregnancy.
Since most Müllerian anomalies are congenital and caused by genetic or developmental factors, they cannot be prevented. However, early detection through imaging and genetic counseling can help manage symptoms and provide appropriate care.
Many women with mild Müllerian anomalies can have a normal pregnancy, but some types may be associated with complications such as:
Most Müllerian anomalies are not inherited. However, there is some evidence that certain anomalies, such as Mayer-Rokitansky-Küster-Hauser syndrome (MRKH), can run in families, suggesting a possible genetic component. Genetic counseling may be recommended for women with a known history of Müllerian anomalies.
MRKH syndrome is a type of Müllerian anomaly where a girl is born with an underdeveloped or absent uterus and upper two-thirds of the vagina. Women with MRKH usually have normal ovaries and external genitalia but are unable to carry a pregnancy. Some women may undergo vaginal reconstruction or other fertility treatments to help them have biological children.
In many cases, women with Müllerian anomalies can have a normal sex life. However, those with certain conditions like MRKH may experience difficulties related to vaginal absence or underdevelopment. Vaginal reconstruction surgery can help improve sexual function for women with MRKH.
The outlook depends on the type and severity of the anomaly: