A slowly progressive hereditary disorder characterized by abnormal accumulations of iron pigments in certain regions of the basal ganglia (eg, globus pallidus and substantia nigra). This autosomal recessive disorder typically becomes apparent during late childhood or adolescence. ...

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Hallervorden-Spatz Disease
... What is Hallervorden-Spatz Disease? Hallervorden-Spatz disease, also called Neurodegeneration with Brain Iron Accumulation, is a rare, inherited, neurological movement disorder characterized by progre...
Source: Cleveland Clinic

Hallervorden-Spatz Disease Information Page
... Hallervorden-Spatz disease, also called Neurodegeneration with Brain Iron Accumulation, is a rare, inherited, neurological movement disorder characterized by progressive degeneration of the nervous sy...
Source: National Institute of Neurological Disorders and Stroke

   

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