0000000000673025
AUTHOR
M. Beneyto
showing 3 related works from this author
El asesoramiento genético en los déficits visuales y auditivos
2008
espanolObjetivo: Las enfermedades hereditarias que afectan a la retina y la audicion presentan una amplia heterogeneidad clinica y genetica. Durante la pasada decada se han producido importantes avances en el conocimiento de la patogenia molecular de estas enfermedades y, actualmente, mas de 200 genes y loci estan implicados en enfermedades de la retina y mas de 60 son responsables de perdida de audicion. Metodo: El estudio genetico molecular es crucial para confirmar el diagnostico clinico, permite, en ocasiones, conocer el pronostico de la enfermedad, un consejo genetico y reproductivo adecuado y permite la posibilidad de crear grupos de pacientes geneticamente homogeneos para futuros ens…
Estudio genético molecular del síndrome de Usher en España
2005
Usher syndrome (USH) associates deafness and retinitis pigmentosa (RP). It is a disease both clinically and genetically heterogeneous. It is inherited as an autosomal recessive trait and its prevalence makes it the most frequent association of hearing loss and RP. Clinically Usher syndrome is divided into type I (USH1), II (USH2) and III (USH3), according to the severity of hearing loss, age of onset of RP and the existence or not of vestibular dysfunction. There are at least 7 different localizations for USH1 and 5 genes have been identified. For USH2, 3 loci and 2 genes have been reported and USH3 is due to Clarin-1 gene. Our aim is to perform a clinical and genetic characterization of al…
Epidemiology of retinitis pigmentosa in the valencian community (Spain)
1995
The purposes of this study are to determine the frequencies of the different genetic forms of retinitis pigmentosa and to perform segregation analysis in the different genetic subtypes. Retinitis pigmentosa was diagnosed in 263 persons from 132 families. The frequency of the autosomal recessive type was the highest (31.8%) while the X-linked type was very rare (1.5%). The frequency of autosomal dominant type was 14.4% and the simplex cases constituted half of the total cases of RP registered in our community. In conclusion, in our population the high proportion of simplex cases and the low number of X-linked families are noticeable. The result of segregation analysis showed good agreement w…