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Enfermedad de Hallervorden-Spatz - Overview

Nombres alternativos

Neurodegeneración asociada a pantotenato cinasa

Definición:

Es un trastorno del movimiento que se transmite de padres a hijos (hereditario).

Causas, incidencia y factores de riesgo:

La enfermedad de Hallervorden-Spatz generalmente comienza en la infancia.

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

Reviewed last on: 9/28/2010
David C. Dugdale, III, MD, Professor of Medicine, Division of General Medicine, Department of Medicine, University of Washington School of Medicine; Daniel B. Hoch, PhD, MD, Assistant Professor of Neurology, Harvard Medical School, Department of Neurology, Massachusetts General Hospital. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

Referencias

Lang A. Other movement disorders. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 434.

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