Article
A French experience of type 3 Gaucher disease: Phenotypic diversity and neurological outcome of 10 patients.
Brain & development - 1 Feb 2011
Kraoua Ichraf, Sedel Frédéric, Caillaud Catherine, Froissart Roseline, Stirnemann Jérôme, Chaurand Guy, Flodrops Hugues, Tari Saliha, Gourfinkel-An Isabelle, Mathieu Sophie, Belmatoug Nadia, Billette de Villemeur Thierry, Mignot Cyril
Abstract excerpt
OBJECTIVE: To describe the clinical presentation of 10 patients with type 3 Gaucher disease and the clinical evolution of nine of them following specific therapy regimes. METHODS: The follow-up of these 10 patients was between 2 and 15 years. The clinical history was provided by each patient's general practitioner and a final clinical evaluation was made by two different physicians including a neurologist. One...
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