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Volumn 37, Issue 3, 1996, Pages 284-286

Cutis verticis gyrata-mental deficiency syndrome: A patient with drug-resistant epilepsy and polymicrogyria

Author keywords

Cutis verticis gyrata; Epilepsy; Mental retardation; Neuroradiology; Polymicrogyria

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 16Q; CHROMOSOME 3P; CHROMOSOME BREAKAGE; CLINICAL FEATURE; DISEASE ASSOCIATION; EPILEPSY; GENETIC ANALYSIS; HUMAN; MALE; MENTAL DEFICIENCY; MICROGYRIA; PRIORITY JOURNAL; SKIN DISEASE;

EID: 0030050762     PISSN: 00139580     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1528-1157.1996.tb00027.x     Document Type: Article
Times cited : (13)

References (14)
  • 1
    • 2842529418 scopus 로고
    • Cutis verticis gyrata
    • Rook A, Wilkinson DS, Ebling FJG, eds. Oxford: Blackwell Scientific Publications
    • Ebling FJG, Rook A. Cutis verticis gyrata. In: Rook A, Wilkinson DS, Ebling FJG, eds. Textbook of dermatology, vol. 2. Oxford: Blackwell Scientific Publications, 1979: 1821-2.
    • (1979) Textbook of Dermatology , vol.2 , pp. 1821-1822
    • Ebling, F.J.G.1    Rook, A.2
  • 2
    • 0002544992 scopus 로고
    • Case of abnormal development of the scalp
    • McDowall TW. Case of abnormal development of the scalp. J Ment Sci 1893;39:62-4.
    • (1893) J Ment Sci , vol.39 , pp. 62-64
    • McDowall, T.W.1
  • 3
    • 0003168887 scopus 로고
    • Cutis verticis gyrata and mental deficiency in Sweden: 1. Epidemiologic and clinical aspects
    • Akesson HO. Cutis verticis gyrata and mental deficiency in Sweden: 1. Epidemiologic and clinical aspects. Acta Med Scand 1964;175:115-27.
    • (1964) Acta Med Scand , vol.175 , pp. 115-127
    • Akesson, H.O.1
  • 4
    • 0002859529 scopus 로고
    • Cutis verticis gyrata, thyroaplasia and mental deficiency
    • Akesson HO. Cutis verticis gyrata, thyroaplasia and mental deficiency. Acta Genet Med (Roma) 1965;14:200-4.
    • (1965) Acta Genet Med (Roma) , vol.14 , pp. 200-204
    • Akesson, H.O.1
  • 6
    • 0003168886 scopus 로고
    • Cutis verticis gyrata and mental deficiency in Sweden. II. Genetic aspects
    • Akesson HO. Cutis verticis gyrata and mental deficiency in Sweden. II. Genetic aspects. Acta Med Scand 1965;177:459-64.
    • (1965) Acta Med Scand , vol.177 , pp. 459-464
    • Akesson, H.O.1
  • 7
    • 2842562814 scopus 로고
    • Cutis verticis gyrata: Studio neurofisiologico e neuroradiologico di un case
    • Musurneci SA, Colognola RM, Ferri R, et al. Cutis verticis gyrata: studio neurofisiologico e neuroradiologico di un case. Boll Lega Ital Epil 1986;54/55:161-3.
    • (1986) Boll Lega Ital Epil , vol.54-55 , pp. 161-163
    • Musurneci, S.A.1    Colognola, R.M.2    Ferri, R.3
  • 8
    • 0024323235 scopus 로고
    • Association of cutis verticis gyrata with fragile X syndrome and fragility of chromosome 12
    • Schepis C, Palazzo R, Ragusa RM, Spina E, Barletta C. Association of cutis verticis gyrata with fragile X syndrome and fragility of chromosome 12. Lancet 1989;2:279.
    • (1989) Lancet , vol.2 , pp. 279
    • Schepis, C.1    Palazzo, R.2    Ragusa, R.M.3    Spina, E.4    Barletta, C.5
  • 9
    • 0026020896 scopus 로고
    • Cutis verticis gyrata and chromosomal fragile sites
    • Musumeci SA, Ferri R, Viglianesi M, et al. Cutis verticis gyrata and chromosomal fragile sites. Am J Med Genet 1991, 38:249-50.
    • (1991) Am J Med Genet , vol.38 , pp. 249-250
    • Musumeci, S.A.1    Ferri, R.2    Viglianesi, M.3
  • 10
    • 84942384712 scopus 로고
    • Curtis verticis gyrata and chromosomal abnormalities
    • Marini R, Cappa M, Neri G. Curtis verticis gyrata and chromosomal abnormalities. Am J Dis Child 1989;143:269-70.
    • (1989) Am J Dis Child , vol.143 , pp. 269-270
    • Marini, R.1    Cappa, M.2    Neri, G.3
  • 11
    • 0019459746 scopus 로고
    • FUdR induction of the X chromosome fragile site: Evidence for the mechanism of folic acid and thymidine inhibition
    • Glover TW. FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition. Am J Hum Genet 1981;33:234-42.
    • (1981) Am J Hum Genet , vol.33 , pp. 234-242
    • Glover, T.W.1
  • 12
    • 0025905795 scopus 로고
    • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
    • Verkerk AJMH, Pieretti M, Sutcliffe SS, et al. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 1991;65:905-14.
    • (1991) Cell , vol.65 , pp. 905-914
    • Verkerk, A.J.M.H.1    Pieretti, M.2    Sutcliffe, S.S.3
  • 13
    • 0014754028 scopus 로고
    • Aetiological aspects of the cutis verticis gyrata and mental retardation syndrome
    • Palo J, Ivanoinen M, Blomquist K, Pesonen S. Aetiological aspects of the cutis verticis gyrata and mental retardation syndrome. J Ment Defic Res 1970;14:33.
    • (1970) J Ment Defic Res , vol.14 , pp. 33
    • Palo, J.1    Ivanoinen, M.2    Blomquist, K.3    Pesonen, S.4
  • 14
    • 0028303886 scopus 로고
    • Magnetic resonance imaging in developmental disorders of the cerebral cortex
    • Kuzniecky RI. Magnetic resonance imaging in developmental disorders of the cerebral cortex. Epilepsia 1994,35 (suppl):S44-56.
    • (1994) Epilepsia , vol.35 , Issue.SUPPL.
    • Kuzniecky, R.I.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.