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Volumn 32, Issue 2, 2014, Pages 160-163

Seckel syndrome: A rare case report

Author keywords

Bird headed appearance; dwarfism; microcephaly; seckel syndrome

Indexed keywords

CASE REPORT; CHILD; HUMAN; MALE; MULTIPLE MALFORMATION SYNDROME; PATHOPHYSIOLOGY; SYNDROME;

EID: 84899050262     PISSN: 09704388     EISSN: 19983905     Source Type: Journal    
DOI: 10.4103/0970-4388.130983     Document Type: Article
Times cited : (7)

References (16)
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    • 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;70:155-8.
    • (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
  • 4
    • 84877788449 scopus 로고    scopus 로고
    • [Last accessed on Jul 18]
    • Faivre L, Cormier-Daire V. Seckel syndrome. Available from: http://www.otpha.net/data/patho/GB/uk-Seckel(05).pdf [Last accessed on 2013 Jul 18].
    • (2013) Seckel Syndrome
    • Faivre, L.1    Cormier-Daire, V.2
  • 6
    • 84899119675 scopus 로고    scopus 로고
    • [Last accessed on Feb 14]
    • Available from: "www.bhopal.net/delhi-marchers/factsheets/ next%20generation.pdf". [Last accessed on 2014 Feb 14].
    • (2014)
  • 11
    • 80155149580 scopus 로고    scopus 로고
    • A recurrent mutation in Moroccan patients with Dyggve-Melchior- Clausensyndrome: Report of a new case and review
    • Elalaoui SC, Mariam T, Ilham R, Yassamine D, Abdelaziz S. A recurrent mutation in Moroccan patients with Dyggve-Melchior-Clausensyndrome: Report of a new case and review. Indian J Hum Genet 2011;17:97-9.
    • (2011) Indian J Hum Genet , vol.17 , pp. 97-99
    • Elalaoui, S.C.1    Mariam, T.2    Ilham, R.3    Yassamine, D.4    Abdelaziz, S.5
  • 12
    • 33749532322 scopus 로고    scopus 로고
    • Seckel syndrome associated with oligodontia, microdontia, enamel hypoplasia, delayed eruption, and dentin dysmineralization: A new variant?
    • De Coster PJ, Verbeec KRM, Holthaus V, Martens LC, Vral A. Seckel syndrome associated with oligodontia, microdontia, enamel hypoplasia, delayed eruption, and dentin dysmineralization: A new variant? J Oral Pathol Med 2006;35:639-41.
    • (2006) J Oral Pathol Med , vol.35 , pp. 639-641
    • De Coster, P.J.1    Verbeec, K.R.M.2    Holthaus, V.3    Martens, L.C.4    Vral, A.5
  • 14
    • 17944382232 scopus 로고    scopus 로고
    • Craniofacial morphology, dentition and skeletal maturity in four siblings with Seckel syndrome
    • Kjaer I, Hansen N, Becktor KB, Birkebaek N, Balslev T. Craniofacial morphology, dentition and skeletal maturity in four siblings with Seckel syndrome. Cleft Palate Craniofac J 2001;38:645-51.
    • (2001) Cleft Palate Craniofac J , vol.38 , pp. 645-651
    • Kjaer, I.1    Hansen, N.2    Becktor, K.B.3    Birkebaek, N.4    Balslev, T.5
  • 15
    • 0037712535 scopus 로고    scopus 로고
    • T-cell clonality and myelodysplasia without chromosomal fragility in a patient with features of Seckel syndrome
    • Chanan-Khan A, Holkova B, Perle MA, Reich E, Wu CD, Inghirami G, et al. T-cell clonality and myelodysplasia without chromosomal fragility in a patient with features of Seckel syndrome. Haematologica 2003;88:ECR14.
    • (2003) Haematologica , vol.88
    • Chanan-Khan, A.1    Holkova, B.2    Perle, M.A.3    Reich, E.4    Wu, C.D.5    Inghirami, G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.