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Volumn 40, Issue 5, 2003, Pages 299-301

Retinal features in Seckel's syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRACHYCEPHALY; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; EYE AXIS LENGTH; FEMALE; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HYPERMETROPIA; INTELLIGENCE QUOTIENT; MANDIBLE HYPOPLASIA; MAXILLA HYPOPLASIA; NYSTAGMUS; OPHTHALMOSCOPY; PHYSICAL EXAMINATION; RETINA DISEASE; RETINA EXAMINATION; RETINA MACULA DEGENERATION; RETINA MACULOPATHY; SCHOOL CHILD; SECKEL SYNDROME; VISUAL ACUITY;

EID: 0141763698     PISSN: 01913913     EISSN: None     Source Type: Journal    
DOI: 10.3928/0191-3913-20030901-12     Document Type: Article
Times cited : (5)

References (12)
  • 2
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    • Seckel syndrome: An overdiagnosed syndrome
    • Thompson E, Pembrey M. Seckel syndrome: an overdiagnosed syndrome. J Med Genet 1985;22:192-201.
    • (1985) J Med Genet , vol.22 , pp. 192-201
    • Thompson, E.1    Pembrey, M.2
  • 3
    • 0023278875 scopus 로고
    • Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage?
    • Butler MG, Hall BD, Maclean RN, Lozzio CB. Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage? Am J Med Genet 1987;27:645-649.
    • (1987) Am J Med Genet , vol.27 , pp. 645-649
    • Butler, M.G.1    Hall, B.D.2    Maclean, R.N.3    Lozzio, C.B.4
  • 4
    • 0028932879 scopus 로고
    • Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instability
    • Syrrou M, Georgiou I, Paschopoulos M, Lolis D. Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instability. Genet Couns 1995;6:37-41.
    • (1995) Genet Couns , vol.6 , pp. 37-41
    • Syrrou, M.1    Georgiou, I.2    Paschopoulos, M.3    Lolis, D.4
  • 7
    • 0034969925 scopus 로고    scopus 로고
    • Seckel's syndrome and malformations of cortical development: Report of three new cases and review of the literature
    • Capovilla G, Lorenzetti ME, Montagnini A, et al. Seckel's syndrome and malformations of cortical development: report of three new cases and review of the literature. J Child Neurol 2001;16:382-386.
    • (2001) J Child Neurol , vol.16 , pp. 382-386
    • Capovilla, G.1    Lorenzetti, M.E.2    Montagnini, A.3
  • 10
    • 0015767312 scopus 로고
    • Ocular anomalies in Seckel's syndrome
    • Lim KH, Wong HB. Ocular anomalies in Seckel's syndrome. Aust N Z J Med 1973;3:520-522.
    • (1973) Aust N Z J Med , vol.3 , pp. 520-522
    • Lim, K.H.1    Wong, H.B.2
  • 11
    • 0030941125 scopus 로고    scopus 로고
    • Central nervous system anomalies in Seckel syndrome: Report of a new family and review of the literature
    • Shanske A, Caride DG, Menasse-Palmer L, Bogdanow A, Marion RW. Central nervous system anomalies in Seckel syndrome: report of a new family and review of the literature. Am J Med Genet 1997;70:155-158.
    • (1997) Am J Med Genet , vol.70 , pp. 155-158
    • Shanske, A.1    Caride, D.G.2    Menasse-Palmer, L.3    Bogdanow, A.4    Marion, R.W.5
  • 12
    • 0032981383 scopus 로고    scopus 로고
    • Severe hypertensive sequelae in a child with Seckel syndrome (bird-like dwarfism)
    • Sorof JM, Dow-Smith C, Moore PJ. Severe hypertensive sequelae in a child with Seckel syndrome (bird-like dwarfism). Pediatr Nephrol 1999;13:343-346.
    • (1999) Pediatr Nephrol , vol.13 , pp. 343-346
    • Sorof, J.M.1    Dow-Smith, C.2    Moore, P.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.