Comprehensive Diagnosis and Treatment of Cloacal Malformations

Received: 2025-05-15

Published: 2025-05-03

Abstract










Cloacal malformation (CM) is a rare and complex congenital anomaly characterized by the fusion of the rectum, vagina, and urethra into a single channel that opens through a single perineal orifice. The incidence is approximately 1 case per 20,000 to 50,000 newborn girls. Timely diagnosis and adequate surgical correction of CM are critically important to ensure normal pelvic organ function and improve the quality of life of patients.










List of references

About the Authors

Ergashev N.Sh.
National Children's Medical Center
Umarov K.M.
National Children's Medical Center
Bobokulov I.Kh.
National Children's Medical Center
Nasirov M.M.
National Children's Medical Center
Abduazizov M.A.
National Children's Medical Center
Yuldashev M.E.
National Children's Medical Center
Dustmuradov J.A.
National Children's Medical Center

How to Cite

Comprehensive Diagnosis and Treatment of Cloacal Malformations. (2025). Herald of the National Children’s Medical Center, 86-88. https://hnchmc.uz/jour/article/view/150

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ISSN 2181-3353 (Print)
ISSN 2181-3353 (Online)