The transition between the phenotypes of Prader-Willi syndrome during infancy and early childhood

Developmental Medicine and Child Neurology

Volumn 52, Issue 6, 2010, Pages 506-507

  Thomson, Allyson Kay ^a  

^a EDITH COWAN UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

GROWTH HORMONE;

ACCESS TO INFORMATION; BEHAVIOR; BODY MASS; CAREGIVER; CHILDHOOD; CLINICAL FEATURE; COGNITION; FAILURE TO THRIVE; FEEDING BEHAVIOR; HUMAN; HYPERPHAGIA; INFANCY; NOTE; PATHOGENESIS; PHENOTYPE; PRACTICE GUIDELINE; PRADER WILLI SYNDROME; PRIORITY JOURNAL;

AGING; CHILD, PRESCHOOL; DISEASE PROGRESSION; FAILURE TO THRIVE; FEEDING BEHAVIOR; HUMANS; HYPERPHAGIA; INFANT; OBESITY; PHENOTYPE; PRADER-WILLI SYNDROME;

EID: 77953934857     PISSN: 00121622     EISSN: 14698749     Source Type: Journal    
DOI: 10.1111/j.1469-8749.2009.03517.x     Document Type: Note

References (5)

1. Cassidy SB, Driscoll DJ. Prader-Willi syndrome. Eur J Hum Genet 2009, 17:3-14.
2. Eiholzer U, L'Allemand D, Schlumpf M, Rousson V, Gasser T, Fusch C. Growth hormone and body composition in children younger than 2 years with Prader-Willi syndrome. J Pediatr 2004, 144:753-8.
3. Holland A, Whittington J, Hinton E. The paradox of Prader-Willi syndrome: a genetic model of starvation. Lancet 2003, 362:989-91.
4. Butler JV, Whittington JE, Holland AJ, McAllister CJ, Goldstone AP. The transition between the phenotypes of Prader-Willi syndrome during infancy and early childhood. Dev Med Child Neurol 10.1111/j.1469-8749.2009.03530.x, (Published online) DOI
5. Russell H, Oliver C. The assessment of food-related problems in individuals with Prader-Willi syndrome. Br J Clin Psychol 2003, 42:379-92.