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Two Ethnic Clusters with Huntington Disease in Israel: The Case of Mountain Jews and Karaites.
Neurodegener Dis ; 17(6): 281-285, 2017.
Article en En | MEDLINE | ID: mdl-28848105
ABSTRACT

BACKGROUND:

Worldwide prevalence estimates of Huntington disease (HD) vary widely, with no reliable information regarding the Jewish population in Israel.

METHODS:

This specialized tertiary single-center cross-sectional study assessed clinical, cognitive, and demographic characteristics of 84 HD patients who were treated at the Movement Disorder Unit of the Tel Aviv Medical Center, Israel.

RESULTS:

Our cohort was composed of one-third Ashkenazi Jews, 27% Mountain Jews (Caucasus Jews), 18% Sephardi Jews, and 21% Karaites, with both Mountain Jews and Karaites over-represented compared to their relevant proportion in the population of the state of Israel, which is less than 1%. No between-group differences were detected regarding the number of CAG (cytosine-adenine-guanine) repeats, age at onset, disease duration, years from symptom onset to diagnosis, gender, years of education, Unified Huntington Disease Rating Scale scores, or the Montreal Cognitive Assessment scores.

CONCLUSION:

We detected clustering of HD among the population treated at our Medical Center, which has the only specialized HD clinic in the country, with a high percentage of HD among 2 relatively small subpopulations of Jews Mountain Jews and Karaites.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Etnicidad / Judíos / Enfermedad de Huntington / Repeticiones de Trinucleótidos / Proteína Huntingtina Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Neurodegener Dis Asunto de la revista: NEUROLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Israel

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Etnicidad / Judíos / Enfermedad de Huntington / Repeticiones de Trinucleótidos / Proteína Huntingtina Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Neurodegener Dis Asunto de la revista: NEUROLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Israel