UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration.
Ann Neurol
; 75(5): 793-798, 2014 May.
Article
in En
| MEDLINE
| ID: mdl-24771548
ABSTRACT
We report a 5-generation family with phenotypically diverse neurodegenerative disease including relentlessly progressive choreoathetoid movements, dysarthria, dysphagia, spastic paralysis, and behavioral dementia in descendants of a 67-year-old woman with amyotrophic lateral sclerosis. Disease onset varied with gender, occurring in male children and adult women. Exome sequence analyses revealed a novel mutation (c.1490C>T, p.P497L) in the ubiquilin-2 gene (UBQLN2) with X-linked inheritance in all studied affected individuals. As ubiquilin-2-positive inclusions were identified in brain, we suggest that mutant peptide predisposes to protein misfolding and accumulation. Our findings expand the spectrum of neurodegenerative phenotypes caused by UBQLN2 mutations.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Ubiquitins
/
Genetic Heterogeneity
/
Cell Cycle Proteins
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Heredodegenerative Disorders, Nervous System
/
Mutation
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Aged
/
Child, preschool
/
Female
/
Humans
/
Male
Language:
En
Journal:
Ann Neurol
Year:
2014
Document type:
Article
Affiliation country:
Morocco