Lethal dilated cardiomyopathy due to long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency
1996; Springer Science+Business Media; Volume: 19; Issue: 3 Linguagem: Galês
10.1007/bf01799273
ISSN1573-2665
AutoresEsmeralda Martins, Alfredo Costa, Ermelinda Santos Silva, M. Medina, Maria Luı́s Cardoso, Christine Vianey‐Saban, P. Divry, Laura Vilarinho,
Tópico(s)Cardiovascular Function and Risk Factors
ResumoJournal of Inherited Metabolic DiseaseVolume 19, Issue 3 p. 373-374 Case Report Lethal dilated cardiomyopathy due to long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency E. Martins, E. Martins Hospital de Crianças Maria Pia, PortugalSearch for more papers by this authorA. Costa, A. Costa Hospital de Vale de Sousa, PortugalSearch for more papers by this authorE. Silva, E. Silva Hospital de Crianças Maria Pia, PortugalSearch for more papers by this authorM. Medina, M. Medina Hospital de Crianças Maria Pia, PortugalSearch for more papers by this authorM. L. Cardoso, M. L. Cardoso Instituto de Genética Médica, Praça Pedro Nunes no. 74, Porto, 4050 PortugalSearch for more papers by this authorC. Vianey-Saban, C. Vianey-Saban Hôpital Debrousse, Lyon, FranceSearch for more papers by this authorP. Divry, P. Divry Hôpital Debrousse, Lyon, FranceSearch for more papers by this authorL. Vilarinho, L. Vilarinho Instituto de Genética Médica, Praça Pedro Nunes no. 74, Porto, 4050 PortugalSearch for more papers by this author E. Martins, E. Martins Hospital de Crianças Maria Pia, PortugalSearch for more papers by this authorA. Costa, A. Costa Hospital de Vale de Sousa, PortugalSearch for more papers by this authorE. Silva, E. Silva Hospital de Crianças Maria Pia, PortugalSearch for more papers by this authorM. Medina, M. Medina Hospital de Crianças Maria Pia, PortugalSearch for more papers by this authorM. L. Cardoso, M. L. Cardoso Instituto de Genética Médica, Praça Pedro Nunes no. 74, Porto, 4050 PortugalSearch for more papers by this authorC. Vianey-Saban, C. Vianey-Saban Hôpital Debrousse, Lyon, FranceSearch for more papers by this authorP. Divry, P. Divry Hôpital Debrousse, Lyon, FranceSearch for more papers by this authorL. Vilarinho, L. Vilarinho Instituto de Genética Médica, Praça Pedro Nunes no. 74, Porto, 4050 PortugalSearch for more papers by this author First published: 01 May 1996 https://doi.org/10.1007/BF01799273Citations: 9 Instituto de Genética Médica, Praça Pedro Nunes no. 74, Porto, 4050, Portugal AboutPDF 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 No abstract is available for this article. References 1Hagenfeldt L, Döbeln V, Holme E et al (1990) 3-Hydroxydicarboxylic aciduria — a fatty acid oxidation defect with severe prognosis. J Pediatr, 116: 687– 692. 2Przyrembel H, Jakobs C, Ijlst L et al (1991) Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. J Inher Metab Dis, 14: 674– 680. 3Wanders R, Duran M, Ijlst L, Jager J, vanGennip A (1989) Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase. Lancet, 2: 52– 53. Citing Literature Volume19, Issue3May 1996Pages 373-374 ReferencesRelatedInformation
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