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Article

PRKCG mutation (SCA-14) causing a Ramsay Hunt phenotype.

Movement disorders : official journal of the Movement Disorder Society - 15 May 2007

Visser Jasper E, Bloem Bastiaan R, van de Warrenburg Bart P C

Abstract excerpt

Progressive myoclonic ataxia, also referred to as Ramsay Hunt syndrome, is characterized by a combination of myoclonus and cerebellar ataxia, infrequently accompanied by tonic-clonic seizures. Its differential diagnosis overlaps with progressive myoclonic epilepsy, a syndrome with myoclonus, tonic-clonic seizures, progressive ataxia and dementia. In patients with progressive myoclonic epilepsy, specific diseases...

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Source

Identifiers

PMID: 17343273
DOI: 10.1002/mds.21414

Genes

PRKCG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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