Pericardial effusion in an infant as a first clinical sign of long chain fatty acid beta-oxidation defect

被引:0
作者
Marin Reina, P. [1 ]
Vidal Mico, S. [1 ]
Modesto Alapont, V. [1 ]
Moya Bonora, A. [2 ]
Dalmau, J. [3 ]
机构
[1] Hosp Infantil La Fe, Secc Cuidados Intens Pediat, Valencia, Spain
[2] Hosp Infantil La Fe, Secc Cardiol Pediat, Valencia, Spain
[3] Hosp Infantil La Fe, Secc Metabolopatias, Valencia, Spain
来源
ANALES DE PEDIATRIA | 2010年 / 72卷 / 04期
关键词
D O I
10.1016/j.anpedi.2009.12.008
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:293 / 294
页数:2
相关论文
共 8 条
  • [1] BOHLES H, 2006, DIAGNOSTIC TRATAMIEN, P229
  • [2] Diagnostic approaches to pediatric cardiomyopathy of metabolic genetic etiologies and their relation to therapy
    Cox, Gerald F.
    [J]. PROGRESS IN PEDIATRIC CARDIOLOGY, 2007, 24 (01) : 15 - 25
  • [3] Carnitine supplementation for inborn errors of metabolism
    Nasser, Mona
    Javaheri, Hoda
    Fedorowicz, Zbys
    Noorani, Zaman
    [J]. COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2009, (02):
  • [4] Fuel utilization in patients with very long-chain Acyl-CoA dehydrogenase deficiency
    Orngreen, MC
    Norgaard, MG
    Sacchetti, M
    van Engelen, BGM
    Vissing, J
    [J]. ANNALS OF NEUROLOGY, 2004, 56 (02) : 279 - 282
  • [5] Pena Quintana L, 2001, An Esp Pediatr, V55, P524
  • [6] Cardiomyopathy and pericardial effusion in infancy point to a fatty acid β-oxidation defect after exclusion of an underlying infection
    Spiekerkoetter, U
    Tenenbaum, T
    Heusch, A
    Wendel, U
    [J]. PEDIATRIC CARDIOLOGY, 2003, 24 (03) : 295 - 297
  • [7] Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop
    Spiekerkoetter, U.
    Lindner, M.
    Santer, R.
    Grotzke, M.
    Baumgartner, M. R.
    Boehles, H.
    Das, A.
    Haase, C.
    Hennermann, J. B.
    Karall, D.
    de Klerk, H.
    Knerr, I.
    Koch, H. G.
    Plecko, B.
    Roeschinger, W.
    Schwab, K. O.
    Scheible, D.
    Wijburg, F. A.
    Zschocke, J.
    Mayatepek, E.
    Wendel, U.
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2009, 32 (04) : 498 - 505
  • [8] Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card
    Wood, JC
    Magera, MJ
    Rinaldo, P
    Seashore, MR
    Strauss, AW
    Friedman, A
    [J]. PEDIATRICS, 2001, 108 (01) : E19