History and Physical. Hellervorden Spatz Disease or PKAN is characterized by progressive dystonia, a motor disorder of extrapyramidal type with gait difficulty.
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Sep 12, 2014 · Hallervorden-Spatz disease (HSD) is a rare disorder characterized by progressive extrapyramidal dysfunction and dementia.
Oct 5, 2023 · Pantothenate kinase-associated neurodegeneration (PKAN), formerly called Hallervorden-Spatz Disease (HSD), is a rare disorder characterized ...
It's an inherited neurological disorder. It causes issues with movement. HSD is a very rare but serious condition that worsens over time and can be fatal.
Sep 1, 2023 · Pantothenate kinase-associated neurodegeneration (PKAN), historically also known as Hallervorden-Spatz syndrome, is an autosomal recessive ...
Pantothenate kinase-associated neurodegeneration
Disease
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Pantothenate kinase-associated neurodegeneration, formerly called Hallervorden–Spatz syndrome, is a genetic degenerative disease of the brain that can lead to parkinsonism, dystonia, dementia, and ultimately death. Neurodegeneration in PKAN is... Wikipedia
Hallervorden–Spatz syndrome is an autosomal recessive disorder characterized by dystonia, parkinsonism, and iron accumulation in the brain.
Pantothenate kinase-associated neurodegeneration (PKAN), formerly called Hallervorden–Spatz syndrome, is a genetic degenerative disease of the brain that ...
Sep 10, 2019 · Pantothenate kinase-associated neurodegeneration (PKAN), formerly called Hallervorden-Spatz syndrome, is a rare, inherited neurological movement ...
Jul 23, 2001 · Hallervorden-Spatz syndrome (HSS) is an autosomal recessive neurodegenerative disorder associated with iron accumulation in the brain.
Hallervorden-Spatz syndrome may be the result of an inborn error of metabolism. Future studies of patients with HSS should include catecholamine analyses of ...
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