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Perioperative management of a child with short-chain acyl-CoA dehydrogenase deficiency.

作者信息

Turpin Brian, Tobias Joseph D

机构信息

College of Osteopathic Medicine, University of Health Sciences, Kansas City, MO, USA.

出版信息

Paediatr Anaesth. 2005 Sep;15(9):771-7. doi: 10.1111/j.1460-9592.2005.01507.x.

DOI:10.1111/j.1460-9592.2005.01507.x
PMID:16101709
Abstract

Short-chain acyl-CoA dehydrogenase (SCAD) is a mitochondrial enzyme that catalyzes the dehydrogenation of short chain fatty acids (4 to 6 carbons in length) thereby initiating the cycle of beta-oxidation. This process generates acetyl-CoA, the key substrate for hepatic ketogenesis or ATP production by the Kreb's cycle. A deficiency of SCAD results in the build-up of potentially cytotoxic metabolites including ethylmalonic acid, methylsuccinyl CoA and butyryl-carnitine. The end-organ involvement is heterogeneous, but most commonly includes hypotonia with possible lipid myopathy and developmental delay. Other reported complications include dysmorphic craniofacial features, hypoglycemia, seizures, scoliosis, hypertonia and hyperreflexia, cyclic vomiting and myocardial dysfunction. We present a 23-month-old girl with SCAD deficiency, who required posterior fossa decompression for type 1 Chiari malformation. The potential perioperative implications of SCAD deficiency are reviewed.

摘要

相似文献

1
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2
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引用本文的文献

1
Short-chain acyl-CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms.短链酰基辅酶 A 脱氢酶缺乏症:从基因到细胞病理学及可能的发病机制。
J Inherit Metab Dis. 2017 Sep;40(5):641-655. doi: 10.1007/s10545-017-0047-1. Epub 2017 May 17.
2
Use of propofol for short duration procedures in children with long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiencies.丙泊酚在患有长链3-羟基酰基辅酶A脱氢酶(LCHAD)或三功能蛋白(TFP)缺乏症的儿童短时间手术中的应用。
Mol Genet Metab. 2014 Jun;112(2):139-42. doi: 10.1016/j.ymgme.2014.03.012. Epub 2014 Apr 6.
3
Short-chain acyl-CoA dehydrogenase (SCAD) deficiency: an examination of the medical and neurodevelopmental characteristics of 14 cases identified through newborn screening or clinical symptoms.
短链酰基辅酶A脱氢酶(SCAD)缺乏症:对通过新生儿筛查或临床症状确诊的14例病例的医学和神经发育特征进行的检查。
Mol Genet Metab. 2008 Sep-Oct;95(1-2):39-45. doi: 10.1016/j.ymgme.2008.06.002. Epub 2008 Aug 3.
4
The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level.114例短链酰基辅酶A脱氢酶(SCAD)缺乏症患者的ACADS基因变异谱以错义变异为主,这些变异导致细胞水平上的蛋白质错误折叠。
Hum Genet. 2008 Aug;124(1):43-56. doi: 10.1007/s00439-008-0521-9. Epub 2008 Jun 4.