Clinical features of familial moyamoya disease

Child's Nervous System

Volumn 22, Issue 3, 2006, Pages 258-262

  Nanba, Rina ^a   Kuroda, Satoshi ^a   Tada, Mitsuhiro ^b   Ishikawa, Tatsuya ^a   Houkin, Kiyohiro ^a   Iwasaki, Yoshinobu ^a  

^a HOKKAIDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b HOKKAIDO UNIVERSITY   (Japan)

Author keywords

Age at onset; Anticipation; Familial case; Female predominance; Genetics; Moyamoya disease; Triplet repeat

Indexed keywords

AGE DISTRIBUTION; ARTICLE; BRAIN HEMORRHAGE; CEREBROVASCULAR ACCIDENT; CLINICAL FEATURE; COMPARATIVE STUDY; CONTROLLED STUDY; DISEASE COURSE; DISEASE PREDISPOSITION; FAMILIAL DISEASE; FEMALE; GENE IDENTIFICATION; GENEALOGY; GENETIC SUSCEPTIBILITY; HUMAN; JAPAN; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; MOYAMOYA DISEASE; NEUROPATHOLOGY; ONSET AGE; PEDIGREE; PRIORITY JOURNAL; SEX DIFFERENCE; STATISTICAL ANALYSIS; SUBARACHNOID HEMORRHAGE; TRANSIENT ISCHEMIC ATTACK;

ADOLESCENT; ADULT; AGE OF ONSET; ANTICIPATION, GENETIC; CHILD; DNA REPEAT EXPANSION; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; JAPAN; KAPLAN-MEIERS ESTIMATE; LINKAGE (GENETICS); MALE; MIDDLE AGED; MOYAMOYA DISEASE; PEDIGREE; STATISTICS, NONPARAMETRIC;

EID: 33644533503     PISSN: 02567040     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00381-005-1230-5     Document Type: Article

References (26)

1. Ashley CT Jr, Warren ST (1995) Trinucleotide repeat expansion and human disease. Annu Rev Genet 29:703-728
2. Bromberg JE, Rinkel GJ, Algra A, van Duyn CM, Greebe P, Ramos LM, van Gijn J (1995) Familial subarachnoid hemorrhage: Distinctive features and patterns of inheritance. Ann Neurol 38:929-934
3. Fraser FC (1997) Trinucleotide repeats not the only cause of anticipation. Lancet 350:459-460
4. Goto Y, Yonekawa Y (1992) Worldwide distribution of moyamoya disease. Neurol Med Chir (Tokyo) 32:883-886
5. Graham JF, Matoba A (1997) A survey of moyamoya disease in Hawaii. Clin Neurol Neurosurg 99(Suppl 2):S31-S35
6. Hall JG (1990) Genomic imprinting: Review and relevance to human diseases. Am J Hum Genet 46:857-873
7. Harley HG, Rundle SA, MacMillan JC, Myring J, Brook JD, Crow S, Reardon W, Fenton I, Shaw DJ, Harper PS (1993) Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. Am J Hum Genet 52:1164-1174
8. Ikeda H, Sasaki T, Yoshimoto T, Fukui M, Arinami T (1999) Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26. Am J Hum Genet 64:533-537
9. Inoue TK, Ikezaki K, Sasazuki T, Matsushima T, Fukui M (2000) Linkage analysis of moyamoya disease on chromosome 6. J Child Neurol 15:179-182
10. Kanai N (1992) A genetic study of spontaneous occlusion of the circle of Willis (moyamoya disease). J Tokyo Women Med Univ 62:1227-1258 (in Japanese)
11. Kaneko Y, Imamoto N, Mannoji H, Fukui M (1998) Familial occurrence of moyamoya disease in the mother and four daughters including identical twins. Neurol Med Chir (Tokyo) 38:349-354
12. Lozano AM, Leblanc R (1987) Familial intracranial aneurysms. J Neurosurg 66:522-528
13. Nakao M (2001) Epigenetics: Interaction of DNA methylation and chromatin. Gene 278:25-31
14. Nanba R, Kuroda S, Ishikawa T, Iwasaki Y, Tada M, Kiyohiro H (2004) Familial moyamoya disease-clinical features and current study. No Shinkei Geka 32:7-16
15. Nanba R, Tada M, Kuroda S, Houkin K, Iwasaki Y (2005) Sequence analysis and bioinformatics analysis of chromosome 17q25 in familial moyamoya disease. Childs Nerv Syst 21(1):62-68
16. Norrgard O, Angquist KA, Fodstad H, Forsell A, Lindberg M (1987) Intracranial aneurysms and heredity. Neurosurgery 20:236-239
17. Rainero I, Valfre W, Gentile S, Lo Giudice R, Ferrero M, Savi L, Pinessi L (2002) A comparison of familial and sporadic migraine in a headache clinic population. Funct Neurology 17:193-197
18. Snell RG, MacMillan JC, Cheadle JP, Fenton I, Lazarou LP, Davies P, MacDonald ME, Gusella JF, Harper PS, Shaw DJ (1993) Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease. Nat Genet 4:393-397
19. Suzuki J, Takaku A (1969) Cerebrovascular "moyamoya" disease. Disease showing abnormal net-like vessels in base of brain. Arch Neurol 20:288-299
20. Takahashi A, Sawamura Y, Houkin K, Kamiyama H, Abe H (1993) The cerebrospinal fluid in patients with moyamoya disease (spontaneous occlusion of the circle of Willis) contains high level of basic fibroblast growth factor. Neurosci Lett 160:214-216
21. Torelli P, Manzoni GC (2003) Clinical observations on familial cluster headache. Neurol Sci 24:61-64
22. Wakai K, Tamakoshi A, Ikezaki K, Fukui M, Kawamura T, Aoki R, Kojima M, Lin Y, Ohno Y (1997) Epidemiological features of moyamoya disease in Japan: Findings from a nationwide survey. Clin Neurol Neurosurg 99(Suppl 2):S1-S5
23. Yamada H, Deguchi K, Tanigawara T, Takenaka K, Nishimura Y, Shinoda J, Hattori T, Andoh T, Sakai N (1997) The relationship between moyamoya disease and bacterial infection. Clin Neurol Neurosurg 99(Suppl 2):S221-S224
24. Yamauchi T, Houkin K, Tada M, Abe H (1997) Familial occurrence of moyamoya disease. Clin Neurol Neurosurg 99(Suppl 2):S162-S167
25. Yamauchi T, Tada M, Houkin K, Tanaka T, Nakamura Y, Kuroda S, Abe H, Inoue T, Ikezaki K, Matsushima T, Fukui M (2000) Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25. Stroke 31:930-935
26. Yoshimoto T, Houkin K, Takahashi A, Abe H (1996) Angiogenic factors in moyamoya disease. Stroke 27:2160-2165