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[Neuroacanthocytosis: a diagnosis that should be considered]
Tunisie Medicale [La]. 2011; 89 (3): 282-284
in French | IMEMR | ID: emr-109390
ABSTRACT
Neuroacanthocythosis regroup heterogeneous neurodegenerative diseases. These conditions share neurological, hematological and even systemic features. In spite of the genetic progress, their pathogenesis is still unknown. To report a new case of neuroacanthocythosis. A 37-year-old woman was admitted for orofacial choreatic movement disorder. These movements were associated to dysarthria, lip and tongue mutilation, areflexia and raised plasma creatine kinase level. Examination of blood smear reveled 10% of acanthocytosis. Neuro-acanthocytosis diagnosis, precisely chorea-acanthocytosis, was done. Neuro-acanthocytosis should be considered in any movement disorder in order to attempt a genetic counseling
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Index: IMEMR (Eastern Mediterranean) Main subject: Chorea / Neurodegenerative Diseases / Creatine Kinase / Dysarthria / Movement Disorders Type of study: Case report Limits: Female / Humans Language: French Journal: Tunisie Med. Year: 2011

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Index: IMEMR (Eastern Mediterranean) Main subject: Chorea / Neurodegenerative Diseases / Creatine Kinase / Dysarthria / Movement Disorders Type of study: Case report Limits: Female / Humans Language: French Journal: Tunisie Med. Year: 2011