Ataxia espinocerebelosa tipo 8. Descripción de una familia.

Autores de IIS La Fe

• 

  José María Millán Salvador

  Autor

Participantes ajenos a IIS La Fe

• Sempere AP
• Royo-Vilanova C
• Medrano V

Abstract

Over the past decade, from the genetic point of view, several of the entities included in the group of hereditary ataxias have been identified. We report a Spanish family with type 8 spinocerebellar ataxia (SCA8), one of the most recent hereditary ataxias to be described from the clinical and genetic points of view.