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Archives de pédiatrie
Volume 12, n° 6
pages 650-653 (juin 2005)
Doi : 10.1016/j.arcped.2005.04.063
Dépistage néonatal de la mucoviscidose : problèmes diagnostiques et aspects éthiques des formes frontières
Neonatal screening of cystic fibrosis: diagnostic and ethical problems with mild mutations
 

M. Roussey a, , A. Le Bihannic a, M.P. Audrezet b, M. Blayau c, M. Dagorne d, E. Deneuville a, C. Férec b, H. Journel e, V. Moisan-Petit e, G. Rault f, V. Scotet b, V. Storni f, P. Vigneron e
a CRCM de Rennes, institut de la mère et de l'enfant, hôpital Sud-CHU de Rennes, 16, boulevard de Bulgarie, 35203 Rennes, France 
b Laboratoire de génétique moléculaire de Brest, Brest, France 
c Laboratoire de biologie moléculaire de Rennes, Rennes, France 
d Service de pédiatrie de Saint-Brieuc, Saint-Brieuc, France 
e CRCM de Bretagne-Sud, France 
f CRCM de Roscoff, Roscoff, France 

*Auteur correspondant.

Mots clés : Mucoviscidose, Dépistage néonatal, Mutation CFTR , Test de la sueur

Keywords : Cystic fibrosis, Neonatal screening, CFTR gene mutation, Sweat test




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