Pediatric cloacal anomaly
What is a cloacal anomaly?
During the normal growth process, the baby's urinary tract, rectum, and vagina all separate to form their own openings. A cloacal anomaly (clo·a·ca - anom·a·ly) occurs when these three openings fail to form, resulting in just one opening when the child is born.
How is a cloacal anomaly diagnosed?
Cloacal anomalies are typically diagnosed right after birth, as the baby girl requires immediate treatment to help pass urine and stool. Cloacal anomalies can sometimes be spotted on prenatal ultrasounds.
How is a cloacal anomaly treated?
Cloacal anomaly doctors and providers
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Dai Chung, MD Pediatric Surgeon
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Craig Peters, MD Pediatric Urologist
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Adam Alder, MD Pediatric Surgeon
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Shane Batie, MD Pediatric Urologist
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Nathalie Brewer, MD Pediatric Surgeon
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Natasha Corbitt, MD Pediatric Surgeon
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Diana Diesen, MD Pediatric Surgeon
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David Ewalt, MD Pediatric Urologist
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Barbara Gaines, MD Pediatric Surgeon
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Lauren Gillory, MD Pediatric Surgeon
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Charles Hong, MD Pediatric Surgeon
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Micah Jacobs, MD Pediatric Urologist
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Jason Jarin, MD Pediatric Gynecologist
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Stephen Megison, MD Pediatric Surgeon
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Joseph Murphy, MD Pediatric Surgeon
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Samir Pandya, MD Pediatric Surgeon
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Faisal Qureshi, MD Pediatric Surgeon
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Mark Ryan, MD Pediatric Surgeon
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Bruce Schlomer, MD Pediatric Urologist
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Irina Stanasel, MD Pediatric Urologist
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Sharon Kluger, APRN, PNP-AC/PC Nurse Practitioner - Pediatric Surgery