Prune-Belly Syndrome in Lebanon

متلازمة برون بيلي في لبنان · Syndrome de Prune-Belly au Liban

Prune-belly syndrome is a rare congenital condition involving the abdominal wall, bladder, urinary tract, and often undescended testes. Dr. Anthony Kallas Chemaly provides staged pediatric urology care and kidney-bladder follow-up in Beirut and Mount Lebanon.

Dr. Anthony Kallas Chemaly

Pediatric Urologist · Fellowship-trained in Europe

  • 📍 HDF (Achrafieh) · CMC (Clemenceau) · MLH (Hazmieh)
  • 📞 Clinic: +961 1 398 630
  • WhatsApp: +961 3 551 326
  • 🌐 Arabic · French · English

Medically reviewed by: Dr. Anthony Kallas Chemaly

Last reviewed: April 5, 2026

Sources used on this page: trusted clinical references and pediatric-hospital resources listed below.

What is prune-belly syndrome?

Prune-belly syndrome, also called Eagle-Barrett syndrome or triad syndrome, is a rare congenital condition. The classic triad includes weak or absent abdominal muscles, a large abnormal bladder with urinary tract dilation, and undescended testes in boys.

Signs and associated problems

Many babies are identified before birth on ultrasound because the bladder or kidneys look enlarged. After birth, children may have a wrinkled abdominal wall, urinary tract infections, difficulty emptying the bladder, constipation, and undescended testes. Some children also have orthopedic, bowel, lung, or kidney problems.

How is it diagnosed?

Diagnosis begins with prenatal or postnatal imaging and a detailed physical examination. Kidney and bladder ultrasound, VCUG, blood tests, and careful assessment of kidney function help define the severity of the urinary tract involvement and guide the treatment plan.

Treatment options

Treatment is individualized. Some children need antibiotic prevention for recurrent urinary tract infection, bladder emptying support, orchidopexy for undescended testes, or reconstructive urinary surgery. In more severe cases, long-term bladder and kidney management is the central part of care.

Why follow-up matters

Prune-belly syndrome is not a one-time operation. Children may need repeated reassessment of bladder emptying, continence, infection risk, growth of the kidneys, and overall renal function throughout childhood.

Dr. Kallas Chemaly's approach

Dr. Kallas Chemaly approaches prune-belly syndrome in stages. He focuses on preserving kidney function, helping the bladder empty safely, coordinating the timing of surgery when needed, and guiding families through the long-term roadmap rather than treating only one visible problem.

References

Serving families across Beirut and Mount Lebanon

Dr. Kallas Chemaly sees children from Achrafieh, Gemmayzeh, Saifi, Sodeco, Verdun, Hamra, Clemenceau, Ras Beirut, Rabieh, Mtayleb, Brummana, Beit Mery, Bikfaya, Mansourieh, Kornet Chehwan, Antelias, Dbayeh, Jounieh, Kaslik, Hazmieh, Yarze, and across Keserwan, Metn, and Baabda.

Related Conditions

Undescended TestisVesicoureteral RefluxHydronephrosis

Frequently Asked Questions

No. Some children need staged reconstructive surgery, while others are managed first with infection prevention, bladder-emptying strategies, and close renal follow-up.
Yes. Many cases are first detected on prenatal ultrasound because the bladder, ureters, or kidneys appear enlarged.
Because children with prune-belly syndrome can have chronic bladder emptying problems and upper urinary tract damage, kidney function needs long-term monitoring even after surgery.

Concerned about your child?

Early evaluation leads to better outcomes. Book a consultation with Dr. Kallas Chemaly today.