Nutritional Profile in an Infant with Prader-Willi Syndrome and Cystic Fibrosis at Year One

Norma Terrazas¹, William Klish¹, Ann Scheimann^2,1

Division of Pediatric Gastroenterology and Nutrition, Texas Children’s Hospital, Houston, TX¹, Division of Pediatric Gastroenterology and Nutrition, Johns Hopkins Hospital, Baltimore, MD²

Separately, both Prader-Willi syndrome and Cystic Fibrosis pose significant challenges for nutritional management to optimize growth and development. We will present the medical history, nutritional intake, laboratory data, growth data and anthropometry including body compositional changes for a child with the combined diagnoses of Prader-Willi Syndrome and Cystic Fibrosis during the first year of life.