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Enfermedad de Hallervorden-Spatz - Información general

Definición:

Es un trastorno del movimiento que se transmite a través de familias (hereditario).

Causas, incidencia y factores de riesgo:

Hallervorden-Spatz es una enfermedad que empeora lentamente (degenerativa) y que por lo general se inicia en la niñez. Esta afección involucra rigidez muscular, debilidad y problemas en el movimiento.

La mayoría de los casos de esta enfermedad se deben a un defecto en el gen que produce una proteína llamada pantotenato cinasa 2. Los pacientes con este defecto genético presentan una acumulación de hierro en partes del cerebro, especialmente en los ganglios basales.

  • Fecha de revisión: 8/26/2006
  • Versión en inglés revisada por:Gail A. Kang, M.D., San Francisco VA Parkinson's Disease Research, Education, & Clinical Center, San Francisco, CA. Review provided by VeriMed Healthcare Network.
  • Traducción y localización realizada por: DrTango, Inc
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