Linkage of Familial Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis) to Chromosome 17q25

Author:

Yamauchi Tohru1,Tada Mitsuhiro1,Houkin Kiyohiro1,Tanaka Toshihiro1,Nakamura Yusuke1,Kuroda Satoshi1,Abe Hiroshi1,Inoue Takuya1,Ikezaki Kiyonobu1,Matsushima Toshio1,Fukui Masashi1

Affiliation:

1. From the Section of Neurosurgery, Department of Neuropathophysiology (T.Y, M.T., K.H., S.K., H.A.), and Division of Cell Biology, Cancer Institute (M.T.), Hokkaido University School of Medicine, Sapporo, Japan; Laboratory of Molecular Medicine (T.T., Y.N.), Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan; and Department of Neurosurgery (T.I., K.I., T.M., M.F.), Neurological Institute, Faculty of Medicine, Kyusyu University, Fukuoka, Japan

Abstract

Background and Purpose —Moyamoya disease is a cerebrovascular disease of unknown cause that mainly affects Japanese children. The incidence of familial occurrence accounts for 9% of cases. The characteristic lesions of moyamoya disease are occasionally seen in neurofibromatosis type 1, of which the causative gene ( NF1 ) has been assigned to chromosome 17q11.2. Methods —To determine whether a gene related to moyamoya disease is located on chromosome 17, we conducted microsatellite linkage analyses on 24 families containing 56 patients with moyamoya disease. Leukocyte DNA extracted from the family members was subjected to polymerase chain reaction for a total of 22 microsatellite markers on chromosome 17. The amplified polymerase chain reaction fragments were analyzed with GeneScan on an automated sequencer. Results —Two-point linkage analysis gave a maximum log 10 odds (LOD) score of 3.11 at the recombination fraction of 0.00 for the marker at locus D17S939. The affected pedigree member method also showed a significantly low P value (<1.0×10 −5 ) for the 5 adjacent markers at 17q25. Multipoint linkage analysis also indicated that the disease gene is contained within the 9-cM region of D17S785 to D17S836, with a maximum LOD score of 4.58. Conclusions —A gene for familial moyamoya disease is located on chromosome 17q25.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialised Nursing,Cardiology and Cardiovascular Medicine,Clinical Neurology

Reference20 articles.

1. Worldwide Distribution of Moyamoya Disease

2. Wakai K Tamakoshi A Ohno Y Kawamura T Ikezaki K Fukui M. Epidemiology of spontaneous occlusion of the circle of Willis: results of national epidemiologic survey. In: The Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare Japan: Annual Report 1995 . Tokyo Japan: Ministry of Health and Welfare Japan; 1995:33–37.

3. Fukuyama Y Kanai N Osawa M. Clinical genetic analysis on the moyamoya disease. In: The Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare Japan: Annual Report 1992 . Tokyo Japan: Ministry of Health and Welfare Japan; 1992:141–146.

4. Osawa M Kanai N Kawai M Fukuyama Y. Clinical genetic study on the idiopathic occlusion of the circle of Willis. In: The Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare Japan: Annual Report 1992 . Tokyo Japan: Ministry of Health and Welfare Japan; 1992:147–152.

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