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Persistent cloaca

Persistent cloaca

Medical condition

2 min read

Why this is trending

Interest in “Persistent cloaca” spiked on Wikipedia on 2026-02-25.

Categorised under Science & Nature, this article fits a familiar pattern. Science and technology topics tend to trend after breakthroughs, space missions, health announcements, or widely shared research findings.

GlyphSignal tracks these patterns daily, turning raw Wikipedia traffic data into a curated feed of what the world is curious about. Every spike tells a story.

2026-01-27Peak: 862026-02-25
30-day total: 1,232

Key Takeaways

  • A persistent cloaca is a symptom of a complex anorectal congenital disorder, in which the rectum, vagina, and urinary tract meet and fuse, creating a cloaca, a single common channel.
  • The severity of the condition depends on where the three tracts have joined together.
  • The length of the common channel can be used to judge prognostic outcomes and technical challenges during surgical repair.
  • This type of malformation happens when the embryonic anorectal and urogenital channels fail to separate during the sixth and seventh weeks of gestational development.
  • Diagnosis Diagnosis of a female with a cloaca should be suspected in a female born with an imperforate anus and small looking genitalia.

A persistent cloaca is a symptom of a complex anorectal congenital disorder, in which the rectum, vagina, and urinary tract meet and fuse, creating a cloaca, a single common channel.

Signs and symptoms

Cloacas appear in a wide spectrum of variation in females born with the malformation. The severity of the condition depends on where the three tracts have joined together. The single orifice, called a common channel, may occur varying in length from 1 to 10 cm. The length of the common channel can be used to judge prognostic outcomes and technical challenges during surgical repair. A common channel less than 3 cm in length usually has good sphincter muscles and a well-developed sacrum. This type of malformation happens when the embryonic anorectal and urogenital channels fail to separate during the sixth and seventh weeks of gestational development. Cloacal malformations are rare; they only occur in approximately 1 in 50,000 live births.

Diagnosis

Diagnosis of a female with a cloaca should be suspected in a female born with an imperforate anus and small looking genitalia. The diagnosis can be made clinically with tests like ultrasound, X-rays, voiding cystourethrogram (VCUG) and cloacagram. MRI of the spine and pelvis and endoscopic examinations may also be performed. Failure to identify a cloaca as being present in a newborn may be dangerous, as more than 90% have associated urological problems. The goal for treatment of a female born with cloaca is to achieve bowel control, urinary control, and sexual function, which includes menstruation, sexual intercourse, and possibly pregnancy. Cloacas probably occur in 1 in 20,000 live births.

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Content sourced from Wikipedia under CC BY-SA 4.0

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