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Possible Causes For Hallervorden-Spatz disease - Causes
- Hereditary, Familial, Genetic Disorders
Hallervorden-Spatz disease (PKAN/NBIA)- Synonyms
- Atrophies Pigmentary Pallidal, Atrophy Pigmentary Pallidal, Brain Iron Accumulation Type I Syndrome, degeneration pallidal pigmentary, Degeneration Pigmentary Pallidal, degeneration pigmentary pallidal (progressive), Degenerations Pigmentary Pallidal, HALLERVORDEN SPATZ DIS, Hallervorden Spatz Disease, Hallervorden Spatz Syndrome, Hallervorden-Spatz, Hallervorden-Spatz Syndrome, NBIA 1, NEUROAXONAL DYSTROPHY JUVENILE-ONSET, Pallidal Atrophies Pigmentary, Pallidal Atrophy Pigmentary, Pallidal Degenerations Pigmentary, pallidal pigmentary degeneration, PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION, pigmentary degeneration pallidal, pigmentary degeneration pallidal (progressive), Pigmentary Pallidal Atrophies, Pigmentary pallidal atrophy, Pigmentary pallidal degener, Pigmentary pallidal degeneration, Pigmentary pallidal degeneration (disorder), Pigmentary Pallidal Degenerations, PKAN
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- External Links Related to Hallervorden-Spatz disease - Causes
- Wikipedia
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- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)