CLINICAL NEUROLOGY AND NEUROSURGERY, vol. 99, Suppl., 1997, page S1-S5, ISSN 0303-8467, NLD
WAKAI (K.), TAMAKOSHI (A.), IKEZAKI (K.), FUKUI (M.), KAWAMURA (T.), AOKI (R.), KOJIMA (M.), LIN (Y.), OHNO (Y.)
Department of Preventive Medicine. Nagoya University School of Medicine. Nagoya. JPN, Department of Neurosurgery. Neurological Institute. Kyushu University Faculty of Medicine. Fukuoka. JPN
Copyright (c) 1997 Elsevier Science B.V. All rights reserved.
To estimate an annual number of patients treated for Moyamoya disease in Japan and to describe the clinico-epidemiological features, a nationwide epidemiological survey was conducted in 1995.
The study consisted of two questionnaires, which were distributed to departments randomly selected, of neurosurgery, neurology and pediatrics in hospitals throughout Japan.
The first questionnaire inquired the number of the patients treated in 1994 and the second one detailed clinico-epidemiological information of each patient reported.
Following major epidemiological findings emerged from the study :
(a) The total annual number of patients treated for Moyamoya disease was estimated as 3900 (95% confidence interval (CI) 3500-4400) in Japan 1994, with the prevalence and incidence rates of 3.16 and 0.35 per 100000 population, respectively ;
(b) the sex ratio (females to males) of the patients was 1.8 ;
(c) the peak of age distribution of the patients was observed in 10-14 years old and a smaller peak in their forties ;
(d) the age at onset was under 10 years old in 47.8% of the patients, but some had developed the disease at the age of 25-49 years ;
(e) family history of Moyamoya disease was found in 10.0% of the patients ;
and (f) about 75% of the patients had normal activity of daily life or working ability even before treatment. (...)
Mots-clés BDSP : Groupe âge, Japon, Asie, Prévalence, Incidence, Epidémiologie, Homme, Système nerveux [pathologie], Vaisseau sanguin [pathologie], Appareil circulatoire [pathologie], Vaisseau sanguin encéphale [pathologie]
Mots-clés Pascal : Nishimoto Kudo maladie, Sex ratio, Age apparition, Classe âge, Japon, Asie, Prévalence, Incidence, Epidémiologie, Homme, Système nerveux pathologie, Système nerveux central pathologie, Encéphale pathologie, Vaisseau sanguin pathologie, Appareil circulatoire pathologie, Cérébrovasculaire pathologie
Mots-clés Pascal anglais : Nishimoto Kudo disease, Sex ratio, Age of onset, Age distribution, Japan, Asia, Prevalence, Incidence, Epidemiology, Human, Nervous system diseases, Central nervous system disease, Cerebral disorder, Vascular disease, Cardiovascular disease, Cerebrovascular disease
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Cote : 98-0006950
Code Inist : 002B17C. Création : 17/04/1998.