Neurology · Neurology / Movement disorders; Behavioral neurology
Corticobasal syndrome
also: Corticobasal syndrome (CBS)
Clinical syndrome of asymmetric rigidity, apraxia and cortical sensory loss.
- Specialty
- Neurology
- Subspecialty
- Neurology / Movement disorders; Behavioral neurology
- Sex & age distribution
- Male: affected; Female: slightly more common; Children: no
- Gene(s) involved
- GRN, MAPT, TARDBP
- Alternative names & eponyms
- Corticobasal syndrome (CBS)
- Note
- Overlaps #70
Etiology & mechanism
Heterogeneous pathology: corticobasal degeneration, PSP, Alzheimer disease or FTLD-TDP.
Gene(s) involved (3)
Symptoms & signs (7)
In plain terms, someone with Corticobasal 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
Dravet syndrome
myoclonus
1 shared
Hallervorden–Spatz syndrome
dystonia
1 shared
Hashimoto encephalopathy syndrome
myoclonus
1 shared
Huntington disease phenocopy syndrome
dystonia
1 shared
Immune effector cell-associated neurotoxicity syndrome
aphasia
1 shared
Leigh syndrome
dystonia
1 shared
Lesch–Nyhan syndrome
dystonia
1 shared
MERRF syndrome
myoclonus
1 shared
Opsoclonus–myoclonus syndrome
myoclonus
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