Nutritional and metabolic findings in patients with Prader-Willi syndrome diagnosed in early infancy

Journal of Pediatric Endocrinology and Metabolism

Volumn 25, Issue 11-12, 2012, Pages 1103-1109

  Ma, Yan Yan ^a   Wu, Tong Fei ^a   Liu, Yu Peng ^a   Wang, Qiao ^a   Song, Jin Qing ^a   Song, Fang ^b   Yang, Yan Ling ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

^b CAPITAL INSTITUTE OF PEDIATRICS   (China)

Author keywords

Feeding difficulties; FISH; Prader Willi syndrome

Indexed keywords

ACYLCARNITINE; AMINO ACID; ARGININE; CARBOXYLIC ACID; CHOLESTEROL; MEDIUM CHAIN FATTY ACID; VITAMIN;

AMINO ACID BLOOD LEVEL; ARTICLE; CHOLESTEROL BLOOD LEVEL; CHROMOSOME 15Q; CLINICAL ARTICLE; DEVELOPMENTAL DISORDER; DIET THERAPY; FAILURE TO THRIVE; FEEDING DISORDER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC LINKAGE; GENETIC SCREENING; HUMAN; HYPERAMMONEMIA; HYPOGLYCEMIA; INFANCY; INFANT; KARYOTYPE; KETOACIDOSIS; LIVER DYSFUNCTION; MALE; MALNUTRITION; MOTOR DEVELOPMENT; NEWBORN; NUTRITIONAL STATUS; PHYSICAL DEVELOPMENT; POLYMERASE CHAIN REACTION; PRADER WILLI SYNDROME; PSYCHOMOTOR DEVELOPMENT; SHORT TANDEM REPEAT; TREATMENT RESPONSE; URINALYSIS; VITAMIN SUPPLEMENTATION;

ARGININE; CARBOXYLIC ACIDS; CARNITINE; CHROMOSOMES, HUMAN, PAIR 15; DIET THERAPY; EARLY DIAGNOSIS; FAILURE TO THRIVE; FEMALE; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT NUTRITION DISORDERS; INFANT, NEWBORN; MALE; PRADER-WILLI SYNDROME; TIME-TO-TREATMENT;

EID: 84872913817     PISSN: 0334018X     EISSN: 21910251     Source Type: Journal    
DOI: 10.1515/jpem-2012-0167     Document Type: Article

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