Neurology · Neurology / Neurodegenerative syndromes
Hallervorden–Spatz syndrome
also: Pantothenate kinase-associated neurodegeneration
Brain iron accumulation disorder with dystonia.
- Specialty
- Neurology
- Subspecialty
- Neurology / Neurodegenerative syndromes
- Sex & age distribution
- Male: affected; Female: affected; Children: yes
- Gene(s) involved
- PANK2
- Alternative names & eponyms
- Pantothenate kinase-associated neurodegeneration
Etiology & mechanism
PANK2 loss causing CoA deficiency.
Gene(s) involved (1)
Symptoms & signs (5)
In plain terms, someone with Hallervorden–Spatz syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
1 shared
Abetalipoproteinemia
retinitis pigmentosa
1 shared
Acquired cerebellar syndrome
dysarthria
1 shared
Aicardi–Goutières syndrome
spasticity
1 shared
Bardet–Biedl syndrome
retinitis pigmentosa
1 shared
Brainstem stroke syndrome
dysarthria
1 shared
Corticobasal syndrome
dystonia
1 shared
Foix–Chavany–Marie syndrome
dysarthria
1 shared
Huntington disease phenocopy syndrome
dystonia
1 shared
Leigh syndrome
dystonia
1 shared
Lesch–Nyhan syndrome
dystonia
Shares genes with
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