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Trisomy 13 (Patau syndrome) and craniosynostosis
2011; Wiley; Volume: 155; Issue: 8 Linguagem: Lituano
10.1002/ajmg.a.34086
ISSN1552-4833
AutoresRafael Fabiano Machado Rosa, Rosana C. M. Rosa, José Antônio Monteiro Flores, Daniel T. Chazan, Cristine Dietrich, Mariana Barth de Barth, Vanessa F. Carpes, André Campos da Cunha, Carla Graziadio, Paulo Ricardo Gazzola Zen,
Tópico(s)Craniofacial Disorders and Treatments
ResumoAmerican Journal of Medical Genetics Part AVolume 155, Issue 8 p. 2018-2020 Research Letter Trisomy 13 (Patau syndrome) and craniosynostosis† Rafael F.M. Rosa, Rafael F.M. Rosa Clinical Genetics, Hospital Materno Infantil Presidente Vargas (HMIPV), RS, Brazil Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, BrazilSearch for more papers by this authorRosana C.M. Rosa, Rosana C.M. Rosa Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, BrazilSearch for more papers by this authorJosé A.M. Flores, José A.M. Flores Pediatric Radiology Service, Hospital da Criança Santo Antônio (HCSA)/Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), RS, BrazilSearch for more papers by this authorDaniel T. Chazan, Daniel T. Chazan Pediatrics Service, HMIPV, RS, BrazilSearch for more papers by this authorCristine Dietrich, Cristine Dietrich Fetal Medicine Service, HMIPV, RS, BrazilSearch for more papers by this authorMariana B. de Barth, Mariana B. de Barth Fetal Medicine Service, HMIPV, RS, BrazilSearch for more papers by this authorVanessa F. Carpes, Vanessa F. Carpes Fetal Medicine Service, HMIPV, RS, BrazilSearch for more papers by this authorAndré C. da Cunha, André C. da Cunha Fetal Medicine Service, HMIPV, RS, BrazilSearch for more papers by this authorCarla Graziadio, Carla Graziadio Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil Clinical Genetics, UFCSPA and CHSCPA, RS, BrazilSearch for more papers by this authorPaulo R.G. Zen, Corresponding Author Paulo R.G. Zen [email protected] Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil Clinical Genetics, UFCSPA and CHSCPA, RS, BrazilGenética Clínica—UFCSPA/CHSCPA, Rua Sarmento Leite, 245/403, CEP: 90050-170 Porto Alegre, RS, Brazil.Search for more papers by this author Rafael F.M. Rosa, Rafael F.M. Rosa Clinical Genetics, Hospital Materno Infantil Presidente Vargas (HMIPV), RS, Brazil Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, BrazilSearch for more papers by this authorRosana C.M. Rosa, Rosana C.M. Rosa Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, BrazilSearch for more papers by this authorJosé A.M. Flores, José A.M. Flores Pediatric Radiology Service, Hospital da Criança Santo Antônio (HCSA)/Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), RS, BrazilSearch for more papers by this authorDaniel T. Chazan, Daniel T. Chazan Pediatrics Service, HMIPV, RS, BrazilSearch for more papers by this authorCristine Dietrich, Cristine Dietrich Fetal Medicine Service, HMIPV, RS, BrazilSearch for more papers by this authorMariana B. de Barth, Mariana B. de Barth Fetal Medicine Service, HMIPV, RS, BrazilSearch for more papers by this authorVanessa F. Carpes, Vanessa F. Carpes Fetal Medicine Service, HMIPV, RS, BrazilSearch for more papers by this authorAndré C. da Cunha, André C. da Cunha Fetal Medicine Service, HMIPV, RS, BrazilSearch for more papers by this authorCarla Graziadio, Carla Graziadio Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil Clinical Genetics, UFCSPA and CHSCPA, RS, BrazilSearch for more papers by this authorPaulo R.G. Zen, Corresponding Author Paulo R.G. Zen [email protected] Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil Clinical Genetics, UFCSPA and CHSCPA, RS, BrazilGenética Clínica—UFCSPA/CHSCPA, Rua Sarmento Leite, 245/403, CEP: 90050-170 Porto Alegre, RS, Brazil.Search for more papers by this author First published: 07 July 2011 https://doi.org/10.1002/ajmg.a.34086Citations: 3 † How to Cite this Article: Rosa RFM, Rosa RCM, Flores JAM, Chazan DT, Dietrich C, de Barth MB, Carpes VF, da Cunha AC, Graziadio C, Zen PRG. 2011. Trisomy 13 (Patau syndrome) and craniosynostosis. Am J Med Genet Part A 155:2018–2020. Read 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 REFERENCES Aypar E, Yildirim MS, Sert A, Ciftci I, Odabas D. 2011. A girl with metopic synostosis and trisomy 13 mosaicism: Case report and review of the literature. Am J Med Genet Part A 155A: 638– 641. Carey JC. 2010. Trisomy 18 and trisomy 13 syndromes. In: SB Cassidy, JE Allanson, editors. Management of genetic syndromes, 3rd edition. New York: Wiley-Liss. pp 807– 823. Graham JM Jr. 2006. Craniosynostosis. In: RE Stevenson, JG Hall, editors. Human malformations and related anomalies, 2nd edition. 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Congenital malformations among liveborn infants with trisomies 18 and 13. Am J Med Genet Part A 140A: 1749– 1756. Sullivan PK, Melsen B, Mulliken JB. 1990. Calvarial sutural abnornalities: Metopic synostosis and coronal deformation—An anatomic, three-dimensional radiographic, and pathologic study. Plast Reconstr Surg 86: 1072– 1077. Unal S, Celik FC, Soy D, Ceylaner S, Ceylaner G. 2009. A boy with trisomy 13 presenting with a subtle clinical picture and metopic synostosis. Am J Med Genet Part A 149A: 1608– 1609. Citing Literature Volume155, Issue8August 2011Pages 2018-2020 ReferencesRelatedInformation
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