French database of children and adolescents with Prader-Willi syndrome

Prader-Willi syndrome (PWS) is a rare multisystem genetic disease leading to severe complications mainly related to obesity. We strongly lack information on the natural history of this complex disease and on what factors are involved in its evolution and its outcome. One of the objectives of the Fre...

Full description

Saved in:

Bibliographic Details
Published in:	BMC medical genetics Vol. 9; no. 1; p. 89
Main Authors:	Molinas, Catherine, Cazals, Laurent, Diene, Gwenaelle, Glattard, Melanie, Arnaud, Catherine, Tauber, Maithe
Format:	Journal Article
Language:	English
Published:	England BioMed Central Ltd 02-10-2008 BioMed Central BMC
Subjects:	Adolescent Analysis Child Child, Preschool Cohort Studies Complications and side effects Databases, Factual Diagnosis Female France - epidemiology Humans Infant Infant, Newborn Male Online databases Prader-Willi syndrome Prader-Willi Syndrome - epidemiology Prader-Willi Syndrome - genetics Quality of Life Surveys and Questionnaires France
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Be the first to leave a comment!