Pathologie-biologie · 2012
[Molecular diagnosis of Gaucher disease in Tunisia].
Аннотация на английскомСтатьяНазвание и аннотация: Перевод в очереди
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Cherif W, Ben Turkia H, Ben Rhouma F, Riahi I, Chemli J, Amaral O, Sá Miranda M C, Caillaud C, Kaabachi N, Tebib N, Abdelhak S, Ben Dridi M F
Аннотация
Gaucher disease is a lysosomal storage disorder caused by a deficiency of the enzyme acid β-glucosidase. In order to determine the mutation spectrum in Tunisia, we performed recurrent mutation screening in 30 Tunisian patients with Gaucher disease. Screening of recurrent mutation by PCR/RFLP and direct sequencing had shown that N370S was the most frequent mutation (22/50 mutant alleles, 44%), followed by L444P mutation, which is found in 16% (8/50 mutant alleles). The recombinant allele (RecNciI) represented 14%. Our findings revealed that the genotype N370S/RecNciI was mosst frequent in patients with childhood onset and it was associated with severe visceral involvement. The screening of these three mutations provided a simple tool for molecular diagnosis of Gaucher disease in Tunisian patients and allowed also genetic counselling for their family members.
Предметные рубрики MeSH
AdolescentAdultAge of OnsetChildChild, PreschoolDNA Mutational AnalysisFemaleGaucher DiseaseGenetic Predisposition to DiseaseGenotypeGlucosylceramidaseHumansInfantInfant, NewbornMaleMiddle AgedMolecular Diagnostic TechniquesPolymerase Chain ReactionPolymorphism, Restriction Fragment LengthTunisiaYoung Adult