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[Neuroacanthocytosis: a diagnosis that should be considered]. / Neuroacantheocytoses: un diagnostic à ne pas méconnaître.
Larbi, Thara; Abdallah, Meya; Hamzaoui, Saloua; Gouider, Emna; Ennafaa, Mourad; Harmel, Ali; Gouider, Neziha; Bouslama, Kamel; Ben Dridi, Mohamed; M'rad, Skander.
Afiliação
  • Larbi T; Service de médecine interne, CHU Mongi Slim Sidi Daoud, Tunis, Tunisie.
Tunis Med ; 89(3): 282-4, 2011 Mar.
Article em Fr | MEDLINE | ID: mdl-21387234
ABSTRACT

BACKGROUND:

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.

AIM:

To report a new case of neuroacanthocythosis CASE REPORT 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 choreaacanthocytosis, was done.

CONCLUSION:

Neuro-acanthocytosis should be considered in any movement disorder in order to attempt a genetic counseling.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuroacantocitose Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: Fr Revista: Tunis Med Ano de publicação: 2011 Tipo de documento: Article País de afiliação: Tunísia
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuroacantocitose Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: Fr Revista: Tunis Med Ano de publicação: 2011 Tipo de documento: Article País de afiliação: Tunísia