Hallervorden-Spatz disease is a rare, inherited, neurological movement disorder characterized by progressive degeneration of the nervous system....
This page was last updated on August 30th, 2008
This page was last updated on August 30th, 2008
Hallervorden-Spatz Syndrome (from Basal Ganglia)
Canadian Content » Health » Conditions_and_Diseases » Neurological_Disorders » Brain_Diseases » Basal_Ganglia » Hallervorden-Spatz_Syndrome »
Hallervorden-Spatz Syndrome Association (HSSA)
Contains news, research information, family pages with personal stories, publications and resources, details of fund-raising efforts and association history.
NORD: Neurodegeneration with Brain Iron Accumulation Type 1
Offers synonyms, a general discussion and further resources for the disorder formerly known as Hallervorden-Spatz Syndrome.
MCW HealthLink
An article about Hallervorden-Spatz disease, with an explanation, the symptoms and prognosis.
OMIM National Center for Biotechnology Information.
A clinical synopsis of Hallervorden-Spatz syndrome.
Hallervorden-Spatz Disease
Information sheet compiled by NINDS.
Contains news, research information, family pages with personal stories, publications and resources, details of fund-raising efforts and association history.
Offers synonyms, a general discussion and further resources for the disorder formerly known as Hallervorden-Spatz Syndrome.
An article about Hallervorden-Spatz disease, with an explanation, the symptoms and prognosis.
A clinical synopsis of Hallervorden-Spatz syndrome.
Information sheet compiled by NINDS.
Basal Ganglia >> Hallervorden-Spatz Syndrome yielded other results on Canadian Content:
|
We haven't found any relevant pages yet. |
|
 |
-
