Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1
Details
Serval ID
serval:BIB_96CF10C220B4
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1
Journal
Lancet Neurology
ISSN
1474-4422
Publication state
Published
Issued date
01/2007
Peer-reviewed
Oui
Volume
6
Number
1
Pages
45-55
Notes
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S. --- Old month value: Jan
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S. --- Old month value: Jan
Abstract
Recent advances in our understanding of the clinical and molecular features of the fragile-X mental-retardation 1 gene, FMR1, highlight the importance of single-gene disorders. 15 years after its discovery, FMR1 continues to reveal new and unexpected clinical presentations and molecular mechanisms. Loss of function of FMR1 is a model for neurodevelopmental and behavioural disorders, including mental retardation, autism, anxiety, and mood instability. In addition, overexpression and CNS toxicity of FMR1 mRNA causes a late-onset neurodegenerative disorder, the fragile-X-associated tremor/ataxia syndrome (FXTAS). A similar mechanism is probably involved in premature ovarian failure, which affects up to 20% of female carriers of an altered FMR1 gene.
Keywords
Adult
Ataxia/drug therapy/*etiology
Female
Fragile X Mental Retardation Protein/biosynthesis/*genetics
Fragile X Syndrome/*complications/drug therapy/*genetics
Gene Expression/physiology
Humans
Male
Menopause/genetics/physiology
Middle Aged
Pedigree
RNA, Messenger
Seizures/drug therapy/etiology
Tremor/drug therapy/*etiology
Pubmed
Web of science
Create date
28/02/2008 10:42
Last modification date
20/08/2019 14:58