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Harper's Success Story
08/31/2017 — When Harper was diagnosed with Beckwith Wiedemann Syndrome shortly after birth, her family knew they wanted the best team possible for her tongue reduction surgery. Harper now leads a limitless life thanks to Dr. Chad Perlyn, an expert in treating macroglossia, and the Craniofacial Center at Nicklaus Children’s Hospital.
A happy surgical outcome for family of infant with Beckwith Wiedemann Syndrome
08/29/2017 — 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).

Comunicados de Prensa Relacionados

Boy with Rare, Genetic Syndrome Returns Home to Trinidad After Complex Craniofacial Surgery
07/20/2017 — 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
06/20/2016 — Conference will bring together families and medical professionals to discuss Beckwith-Wiedemann Syndrome treatment and support offerings.