Mutation analysis of KIF21A in congenital fibrosis of the extraocular muscles (CFEOM) patients

Détails

ID Serval
serval:BIB_E33C5FD3A271
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Mutation analysis of KIF21A in congenital fibrosis of the extraocular muscles (CFEOM) patients
Périodique
Ophthalmic Genetics
Auteur(s)
Tiab  L., d'Alleves Manzi  V., Borruat  F. X., Munier  F., Schorderet  D.
ISSN
1381-6810 (Print)
Statut éditorial
Publié
Date de publication
12/2004
Volume
25
Numéro
4
Pages
241-6
Notes
Journal Article --- Old month value: Dec
Résumé
PURPOSE: CFEOM type 1 refers to a group of congenital eye movement disorders that is characterized by nonprogressive ophthalmoplegia affecting all the extraocular muscles. Individuals with the classic form of CFEOM are born with bilateral ptosis, infraducted eyes, and impossibility to raise their eyes above midline. This phenotype is often inherited as an autosomal dominant trait. CFEOM1 maps to the FEOM1 locus on chromosome 12 and is the consequence of mutations in the KIF21A gene. We analyzed three families and one sporadic case for potential genetic heterogeneity. METHODS: Blood samples were collected from members of three families (Swiss, Turkish, and French origin) and one sporadic case (Iranian origin). In families, haplotype was tested for linkage to the autosomal dominant CFEOM1 locus on chromosome 12. Linkage studies were conducted using 2 polymorphic DNA microsatellite markers, D12S331 and D12S1048. Mutation analysis was performed by PCR amplification and bidirectional direct sequencing. RESULTS: Haplotype analysis was compatible with linkage to the CFEOM1 locus in all affected members. Mutation analysis revealed the classical mutation R954W in all affected cases, including the sporadic case, regardless of their ethnic origin. The c.2860C>T base change was not observed in 100 individuals from various ethnic origins. CONCLUSIONS: As reported, the classical c.2860C>T mutation represents a hotspot for mutation in various ethnic groups, including Swiss, Turkish, French, and Iranian patients. Sporadic cases are often due to neo-mutations as in our case. Mutation analysis is important, especially in sporadic cases, to correctly evaluate recurrence and transmission risks.
Mots-clé
Chromosomes, Human, Pair 12/genetics DNA Mutational Analysis Facial Muscles/*innervation/pathology Female Fibrosis Haplotypes/genetics Humans Kinesin/*genetics Linkage (Genetics)/*genetics Male Microsatellite Repeats *Mutation Nerve Tissue Proteins/*genetics Oculomotor Muscles/*innervation/pathology Ophthalmoplegia/congenital/*genetics/pathology Pedigree Phenotype Polymerase Chain Reaction Variation (Genetics)
Pubmed
Création de la notice
28/01/2008 12:59
Dernière modification de la notice
20/08/2019 16:07
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