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http://dx.doi.org/10.4070/kcj.2013.43.1.54

A Case of Congenital Hypertrophic Cardiomyopathy  

Seo, Hyeon Seok (Department of Pediatrics, Korea University Hospital)
Lee, In Hak (Department of Pediatrics, Korea University Hospital)
Song, Young Wooh (Department of Pediatrics, Korea University Hospital)
Choi, Byung Min (Department of Pediatrics, Korea University Hospital)
Jang, Gi Young (Department of Pediatrics, Korea University Hospital)
Son, Chang Sung (Department of Pediatrics, Korea University Hospital)
Lee, Joo Won (Department of Pediatrics, Korea University Hospital)
Publication Information
Korean Circulation Journal / v.43, no.1, 2013 , pp. 54-56 More about this Journal
Abstract
Congenital hypertrophic cardiomyopathy (HCMP) is a very rare congenital heart disease. Here, we report a case of neonatal HCMP, which was confirmed by two-dimensional echocardiography and autopsy. The HCMP rapidly progressed and the patient's condition deteriorated, despite the treatment for congestive heart failure.
Keywords
Cardiomyopathy, hypertrophic; Newborns;
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Times Cited By KSCI : 2  (Citation Analysis)
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1 Kim WW, Shim SH. A case report of Noonan syndrome with mental retardation and attention-deficit hyperactivity disorder. J Korean Acad Child Adolesc Psychiatry 2012;23:31-5.   DOI   ScienceOn
2 Kim J, Kim MR, Kim HJ, Lee KA, Lee MG. LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD. Ann Dermatol 2011;23:232-5.   DOI   ScienceOn
3 Kim JY, Kim MJ, Song ES, Jho YK, Choi YY, Ma JS. Costello syndrome: three sporadic cases. Korean J Pediatr 2007;50:1024-9.   DOI   ScienceOn
4 Badertscher A, Bauersfeld U, Arbenz U, Baumgartner MR, Schinzel A, Balmer C. Cardiomyopathy in newborns and infants: a broad spectrum of aetiologies and poor prognosis. Acta Paediatr 2008;97:1523-8.   DOI   ScienceOn
5 Oh JH, Hong YM, Choi JY, et al. Idiopathic cardiomyopathies in Korean children. - 9-Year Korean Multicenter Study-. Circ J 2011;75:2228-34.   DOI   ScienceOn
6 Fahrner JA, Frazier A, Bachir S, et al. A rasopathy phenotype with severe congenital hypertrophic obstructive cardiomyopathy associated with a PTPN11 mutation and a novel variant in SOS1. Am J Med Genet A 2012;158A:1414-21.   DOI   ScienceOn
7 Berger S, Dhala A, Dearani JA. State-of-the-art management of hypertrophic cardiomyopathy in children. Cardiol Young 2009;19 Suppl 2: 66-73.   DOI   ScienceOn
8 Eidem BW, Jones C, Cetta F. Unusual association of hypertrophic cardiomyopathy with complete atrioventricular canal defect and Down syndrome. Tex Heart Inst J 2000;27:289-91.
9 Somerville J, Becú L. Congenital heart disease associated with hypertrophic cardiomyopathy. Br Heart J 1978;40:1034-9.   DOI