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The Israeli national population program of genetic carrier screening for reproductive purposes.
Zlotogora, Joël; Grotto, Itamar; Kaliner, Ehud; Gamzu, Ronni.
Afiliación
  • Zlotogora J; Department of Community Genetics.
  • Grotto I; Public Health Services.
  • Kaliner E; Ministry of Health, Jerusalem, Israel.
  • Gamzu R; Hadassah Medical School, Hebrew University, Jerusalem, Israel.
Genet Med ; 18(2): 203-6, 2016 Feb.
Article en En | MEDLINE | ID: mdl-25880436
PURPOSE: The Israeli population genetic screening program for reproductive purposes, launched in January 2013, includes all known, nationally frequent severe diseases (carrier frequency 1:60 and/or disease frequency 1 in 15,000 live births). The carrier screening program is free of charge and offers testing for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy for nearly the entire population, according to disease frequency among the different groups within the population. We report the results of the first year of the program. METHODS: Data on the tests performed over a 12-month period were collected from laboratories nationwide. RESULTS: More than 62,000 individuals were examined. The carrier frequency was within the expected range for most of the diseases. The few exceptions included lower carrier rates for cystic fibrosis among Muslim Arabs (1:236) and Druze (1:1,021) and Niemann-Pick type A among Muslim Arabs in a delineated region of Israel (1:229). CONCLUSION: The national population genetic carrier screening is aimed toward providing couples with knowledge of the existing options for the prevention of serious genetic conditions when it is relevant for them. It is still too early to determine whether this aim has been achieved.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pruebas Genéticas / Enfermedades Genéticas Congénitas / Tamización de Portadores Genéticos / Programas Nacionales de Salud Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pruebas Genéticas / Enfermedades Genéticas Congénitas / Tamización de Portadores Genéticos / Programas Nacionales de Salud Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article