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</script>A five-years long study aiming to describe the basic genetic epidemiology of the dystrophinopathies in Costa Rica recruited 31 patients with clinical symptoms of DMD/BMD at the National Children's Hospital (HNN). This center is the obligate reference hospital of the national health system for genetic diseases, however, the geographic origin of the patients, a low percentage of deletions and a high proportion of de novo mutations found among them indicate that a significant ascertainment bias impedes a substantial scientific approach to confront and alleviate the problems posed by these severe diseases in Costa Rica.
muscular dystrophy, Costa Rica, Genetic Markers, Male, haplotypes, X Chromosome, QH301-705.5, Genetic Linkage, carriers, cromosoma X, Distrofia muscular, haplotipos, Polymerase Chain Reaction, Cromosoma X, X chromosome, Humans, Biology (General), deleciones, portadoras, Chromosomes, Human, X, Genetic Carrier Screening, duchenne, deletions, Duchenne, Muscular dystrophy, Enfermedades genéticas, distrofia muscular, Muscular Dystrophy, Duchenne, becker, Haplotypes, Becker, distrofia muscula, Mutation, Female, Haplotipos
muscular dystrophy, Costa Rica, Genetic Markers, Male, haplotypes, X Chromosome, QH301-705.5, Genetic Linkage, carriers, cromosoma X, Distrofia muscular, haplotipos, Polymerase Chain Reaction, Cromosoma X, X chromosome, Humans, Biology (General), deleciones, portadoras, Chromosomes, Human, X, Genetic Carrier Screening, duchenne, deletions, Duchenne, Muscular dystrophy, Enfermedades genéticas, distrofia muscular, Muscular Dystrophy, Duchenne, becker, Haplotypes, Becker, distrofia muscula, Mutation, Female, Haplotipos
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