Prune belly syndrome

Discussion:

Prune belly syndrome is classically described by a triad of clinical features: abdominal wall aplasia/deficiency, urinary tract abnormalities and bilateral cryptorchidism.

This patient reports the diagnosis at birth. Interestingly, this patient engages in paid manual labor despite the absence of abdominal wall musculature.

The diagnosis is based on clinical features. These are commonly identified on the second-trimester antenatal ultrasound.

Differentials include posterior urethral valves and megacystis microcolon intestinal hypoperistalsis syndrome.

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