NR ANAD

AU Zilber,N.; Kahana,E.; Abraham,M.

TI The Libyan Creutzfeldt-Jakob disease focus in Israel: an epidemiologic evaluation.

QU Neurology 1991 Sep; 41(9): 1385-9

PT journal article

AB In a country-wide study of Creutzfeldt-Jakob disease (CJD) in Israel, we diagnosed 114 cases, among them 49 Libyan-born, with onset of their disease during the years 1963-1987. After age adjustment, the mean annual incidence rate per million population was 43 among Libyan-born and 0.9 in the rest of the population. Among Jews born in Egypt and Tunisia, neighboring countries of Libya, the adjusted rates were higher than in the other Israelis (3.5 and 2.3 per million, respectively). Among Libyan Jews, there was no association between incidence rate of CJD and age at immigration, ie, duration of exposure to hypothetical infectious factor in Libya. The percent of familial cases among Libyan Jews (41 to 47%) is one of the highest ever published. Genetic factors seem to be important for the high incidence of CJD among Libyan Jews.

IN Unter lybischen Juden ist die erbliche Creutzfeldt-Jakob-Krankheit etwa 47-fach häufiger als in Israel.

MH Adult; Age Factors; Aged; Creutzfeldt-Jakob Syndrome/*epidemiology/genetics; Female; Human; Israel/epidemiology; Libya/ethnology; Male; Middle Age

AD Department of Neurology, Hadassah University Hospital, Jerusalem, Israel.

SP englisch

PO USA

EA pdf-Datei

Autorenindex - authors index
Startseite - home page