Brain Iron Accumulation Type I Syndrome
[A rare neuroaxonal dystrophy, histologically characterized by axonal spheroids, iron deposition, lewy body (LB)-like intraneuronal inclusions and neurofibrillary tangles. ( NCI )]
UMLS (NCI) C0018523- Disease or Syndrome
Relation/PAR: basal ganglia disease
movement disorder
Neuroaxonal Dystrophies
Heredodegenerative Disorders, Nervous System
movement disorder
Neuroaxonal Dystrophies
Heredodegenerative Disorders, Nervous System
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