Home > Health > Conditions and Diseases > Neurological Disorders > Brain Diseases > Basal Ganglia > Hallervorden-Spatz Syndrome
Hallervorden-Spatz disease is a rare, inherited, neurological movement disorder characterized by progressive degeneration of the nervous system.
http://www.ninds.nih.gov/disorders/nbia/nbia.htm
Information sheet compiled by NINDS.
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Neurodegeneration+with+Brain+Iron+Accumulation+Type+1
Offers synonyms, a general discussion and further resources for the disorder formerly known as Hallervorden-Spatz Syndrome.
Home > Health > Conditions and Diseases > Neurological Disorders > Brain Diseases > Basal Ganglia > Hallervorden-Spatz Syndrome
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