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Neurodegeneration with brain iron accumulation

Neurodegeneration with brain iron accumulation (NBIA, formerly Hallervorden-Spatz syndrome) encompasses a group of rare neurodegenerative disorders characterized by progressive extrapyramidal dysfunction (dystonia, rigidity, choreoathetosis), iron accumulation in the brain and the presence of axonal spheroids, usually limited to the central nervous system.

1 trial tagged with this condition →

Neurodegeneration with brain iron accumulation 5 4 trials
Pantothenate kinase-associated neurodegeneration 4 trials Sub-types →
PLA2G6-associated neurodegeneration 1 trial Sub-types →
Kufor-Rakeb syndrome 0 trials Sub-types →
Woodhouse-Sakati syndrome 0 trials
Aceruloplasminemia 0 trials
Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome 0 trials
Fatty acid hydroxylase-associated neurodegeneration 0 trials
Neurodegeneration with brain iron accumulation 4 0 trials
Neurodegeneration with brain iron accumulation 6 0 trials
Neurodegeneration with brain iron accumulation 7 0 trials
Neurodegeneration with brain iron accumulation 8 0 trials
Neurodegeneration with brain iron accumulation 9 0 trials
Neuroferritinopathy 0 trials