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Finlay–Marks (SEN) syndrome: A sporadic case and the delineation of the syndrome

2006; Wiley; Volume: 140A; Issue: 3 Linguagem: Inglês

10.1002/ajmg.a.31063

ISSN

1552-4833

Autores

Nara Sobreira, Décio Brunoni, Mirlene Cecília Soares Pinho Cernach, Ana Beatriz Alvarez Pérez,

Tópico(s)

Tracheal and airway disorders

Resumo

American Journal of Medical Genetics Part AVolume 140A, Issue 3 p. 300-302 Research Letter Finlay–Marks (SEN) syndrome: A sporadic case and the delineation of the syndrome Nara Lygia de Macena Sobreira, Nara Lygia de Macena Sobreira Departamentos de Morfologia e de Pediatria, Centro de Genética Médica, UNIFESP-EPM, São Paulo, BrazilSearch for more papers by this authorDécio Brunoni, Décio Brunoni Departamentos de Morfologia e de Pediatria, Centro de Genética Médica, UNIFESP-EPM, São Paulo, BrazilSearch for more papers by this authorMirlene Cecília Soares Pinho Cernach, Mirlene Cecília Soares Pinho Cernach Departamentos de Morfologia e de Pediatria, Centro de Genética Médica, UNIFESP-EPM, São Paulo, BrazilSearch for more papers by this authorAna Beatriz Alvarez Perez, Corresponding Author Ana Beatriz Alvarez Perez [email protected] Departamentos de Morfologia e de Pediatria, Centro de Genética Médica, UNIFESP-EPM, São Paulo, BrazilCentro de Genética Médica, UNIFESP-EPM, Rua Coronel Lisboa, 966, 04020-023 São Paulo, Brazil.Search for more papers by this author Nara Lygia de Macena Sobreira, Nara Lygia de Macena Sobreira Departamentos de Morfologia e de Pediatria, Centro de Genética Médica, UNIFESP-EPM, São Paulo, BrazilSearch for more papers by this authorDécio Brunoni, Décio Brunoni Departamentos de Morfologia e de Pediatria, Centro de Genética Médica, UNIFESP-EPM, São Paulo, BrazilSearch for more papers by this authorMirlene Cecília Soares Pinho Cernach, Mirlene Cecília Soares Pinho Cernach Departamentos de Morfologia e de Pediatria, Centro de Genética Médica, UNIFESP-EPM, São Paulo, BrazilSearch for more papers by this authorAna Beatriz Alvarez Perez, Corresponding Author Ana Beatriz Alvarez Perez [email protected] Departamentos de Morfologia e de Pediatria, Centro de Genética Médica, UNIFESP-EPM, São Paulo, BrazilCentro de Genética Médica, UNIFESP-EPM, Rua Coronel Lisboa, 966, 04020-023 São Paulo, Brazil.Search for more papers by this author First published: 12 January 2006 https://doi.org/10.1002/ajmg.a.31063Citations: 11Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat REFERENCES Aase JM, Wilroy SR. 1988. The Finlay–Marks (SEN) syndrome: Report of a new case and review of literature. Proc Greenwood Genet Center 7: 177–178. Baris H, Tan WH, Kimonis VE. 2005. Hypothelia, syndactyly, and ear malformation—A variant of the scalp-ear-nipple syndrome? Case report and review of the literature. Am J Med Genet Part A 134A: 220–222. Edwards MJ, McDonald D, Moore P, Rae J. 1994. Scalp-Ear-Nipple syndrome: Additional manifestations. Am J Med Genet 50: 247–250. Finlay AY, Marks R. 1978. A hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples. Brit J Derm 99: 423–430. Le Merrer M, Renier D, Briard ML. 1991. Scalp defect, nipple absence and ear abnormalities: Another case of Finlay syndrome. Genet Counseling 2: 233–236. Picard C, Couderc S, Skojaei T, Salomon R, de Lonlay P, Le Merrer M, Munnich A, Lyonnet S, Amiel J. 1999. Scalp-ear-nipple (Finlay–Marks) syndrome: A familial case with renal involvement. (Letter) Clin Genet 56: 170–172. Plessis G, Le Treust M, Le Merrer M. 1997. Scalp defect, absence of nipples, ear anomalies, renal hypoplasia: Another case of Finlay–Marks syndrome. Clin Genet 52: 231–234. Taniai H, Chen H, Ursin S. 2004. Finlay–Marks Syndrome: Another sporadic case and additional manifestations. Pediatr Int 46: 353–355. Tuffli GA, Laxova R. 1983. New, autosomal dominant form of ectodermal dysplasia. Am J Med Genet 14: 381–384. Citing Literature Volume140A, Issue31 February 2006Pages 300-302 ReferencesRelatedInformation

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