Prune belly syndrome: a case of early prenatal diagnosis

Authors

  • Suvidhi Kamra Department of Obstetrics and Gynecology, Maharishi Markandeshwar Institute of Medical Sciences and Research, Mullana, Ambala, Haryana, India
  • Unmesh Santpur Department of Obstetrics and Gynecology, Maharishi Markandeshwar Institute of Medical Sciences and Research, Mullana, Ambala, Haryana, India
  • Nidhi Puri Department of Anatomy, Maharishi Markandeshwar Institute of Medical Sciences and Research, Mullana, Ambala, Haryana, India
  • Neetu Pippet Department of Anatomy, Maharishi Markandeshwar Institute of Medical Sciences and Research, Mullana, Ambala, Haryana, India

DOI:

https://doi.org/10.18203/2320-1770.ijrcog20171447

Keywords:

Abdominal wall musculature, Abortus, Cryptoorchidism, Megalourethra, Prune belly syndrome, Ultrasound

Abstract

Prune belly syndrome is a rare congenital disorder typically characterized by a triad of malformation of the urogenital tract, defect of abdominal wall musculature, and cryptorchidism. The condition is generally incompatible with life as infants born with this syndrome are either stillborn or die within the first few weeks of life. The present case is of a fetus presenting with prune bell syndrome, detected in first trimester of pregnancy.

References

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Published

2017-03-30

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Section

Case Reports