Persistent cloaca

Persistent cloaca is a rare birth defect that occurs in female infants, in which the rectum, vagina, and urinary tract meet and fuse, creating a single common channel. This condition is the most severe form of anorectal malformation and is also known as cloacal malformation.

Etiology

The exact cause of persistent cloaca is unknown. However, it is believed to occur during the early stages of pregnancy when the baby's rectum, vagina, and urinary tract are developing. Some researchers suggest that it may be related to genetic factors or environmental influences.

Symptoms

The main symptom of persistent cloaca is the absence of separate openings for the rectum, vagina, and urinary tract in a newborn girl. Other symptoms may include abdominal swelling and difficulties with passing urine or stool.

Diagnosis

Persistent cloaca is usually diagnosed at birth or shortly after. The diagnosis is confirmed through physical examination and imaging tests such as ultrasound, magnetic resonance imaging (MRI), or computed tomography (CT) scan.

Treatment

The treatment for persistent cloaca involves surgery to create separate openings for the rectum, vagina, and urinary tract. The timing and type of surgery depend on the severity of the condition and the baby's overall health. Post-surgery, ongoing care may be needed to manage potential complications and improve the child's quality of life.

Prognosis

The prognosis for girls with persistent cloaca varies. With early diagnosis and appropriate treatment, many can lead normal lives. However, they may face ongoing challenges such as urinary and bowel problems, sexual dysfunction, and psychosocial issues.

See also

• Anorectal malformation
• Birth defect
• Congenital disorder

Persistent cloaca Resources
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