Harper's Success Story


Leer Anterior Leer Próximo

Noticias Relacionadas

A happy surgical outcome for family of infant with Beckwith Wiedemann Syndrome
Alyssa Caulley talks about her experiences at Nicklaus Children's Hospital, where she decided to have her daughter's surgery for Beckwith Wiedemann Syndrome (BWS).
Boy with Rare, Genetic Syndrome Returns Home to Trinidad After Complex Craniofacial Surgery
A team of surgeons from Nicklaus Children’s Hospital’s Craniofacial Center performed a complex reconstructive surgery on a seven year-old child that will improve his vision and ability to eat, as well as his appearance and overall quality of life.

Comunicados de Prensa Relacionados

Boy with Rare, Genetic Syndrome Returns Home to Trinidad After Complex Craniofacial Surgery
A team of surgeons from Nicklaus Children’s Hospital’s Craniofacial Center performed a complex reconstructive surgery on a seven year-old child that will improve his vision and ability to eat, as well as his appearance and overall quality of life.

Nicklaus Children's Hosts Beckwith-Wiedemann Syndrome Conference
Conference will bring together families and medical professionals to discuss Beckwith-Wiedemann Syndrome treatment and support offerings.