Neurology · Neurology / Neuromuscular (inherited neuropathies)
Roussy–Lévy syndrome
also: Roussy–Lévy syndrome
Demyelinating CMT with tremor and areflexia.
- Specialty
- Neurology
- Subspecialty
- Neurology / Neuromuscular (inherited neuropathies)
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes, onset in childhood
- Gene(s) involved
- MPZ, PMP22
- Alternative names & eponyms
- Roussy–Lévy syndrome
Etiology & mechanism
Mutations in myelin proteins.
Gene(s) involved (2)
Symptoms & signs (4)
In plain terms, someone with Roussy–Lévy 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.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
2 shared
Miller Fisher syndrome
areflexia, ataxia
1 shared
Abetalipoproteinemia
ataxia
1 shared
Acquired cerebellar syndrome
ataxia
1 shared
Action myoclonus–renal failure syndrome
ataxia
1 shared
Angelman syndrome
ataxia
1 shared
Brown–Vialetto–Van Laere syndrome
ataxia
1 shared
Cerebral folate deficiency syndrome
ataxia
1 shared
Dandy–Walker malformation
ataxia
1 shared
Dravet syndrome
ataxia
1 shared
EAST syndrome
ataxia
Shares genes with
None.
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