一名患有I型戊二酸血症的儿童反复出现横纹肌溶解症。 - Suppr

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Recurrent rhabdomyolysis in a child with glutaric aciduria type I.

作者信息

Wilson C J, Collins J E, Leonard J V

机构信息

Department of Metabolic Medicine, Great Ormond Street Hospital, London, UK.

出版信息

J Inherit Metab Dis. 1999 Jun;22(5):663-4. doi: 10.1023/a:1005542400135.

DOI:10.1023/a:1005542400135

PMID:10399098

Abstract

摘要

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Recurrent rhabdomyolysis in a child with glutaric aciduria type I.

J Inherit Metab Dis. 1999 Jun;22(5):663-4. doi: 10.1023/a:1005542400135.

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引用本文的文献

Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review.

World J Pediatr. 2016 Aug;12(3):368-371. doi: 10.1007/s12519-016-0042-x. Epub 2016 Jun 29.

Rhabdomyolysis in glutaric aciduria type I.

J Inherit Metab Dis. 2003;26(7):711-2. doi: 10.1023/b:boli.0000005635.89043.8a.

本文引用的文献

Glutaric aciduria type 1 (glutaryl-CoA-dehydrogenase deficiency): advances and unanswered questions. Report from an international meeting.

Eur J Pediatr. 1997 Nov;156(11):821-8. doi: 10.1007/s004310050721.

Myoglobinuria, malignant hyperthermia, neuroleptic malignant syndrome and serotonin syndrome.

Neurol Clin. 1997 Aug;15(3):649-71. doi: 10.1016/s0733-8619(05)70338-8.

Early signs and course of disease of glutaryl-CoA dehydrogenase deficiency.

J Inherit Metab Dis. 1995;18(2):173-6. doi: 10.1007/BF00711759.

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相似文献

Recurrent rhabdomyolysis in a child with glutaric aciduria type I.

J Inherit Metab Dis. 1999 Jun;22(5):663-4. doi: 10.1023/a:1005542400135.

Rhabdomyolysis in glutaric aciduria type I.

J Inherit Metab Dis. 2003;26(7):711-2. doi: 10.1023/b:boli.0000005635.89043.8a.

Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review.

World J Pediatr. 2016 Aug;12(3):368-371. doi: 10.1007/s12519-016-0042-x. Epub 2016 Jun 29.

Macrocephaly, subarachnoid fluid collection, and glutaric aciduria type I.

J Child Neurol. 1996 Sep;11(5):414-7. doi: 10.1177/088307389601100516.

Glutaric aciduria type I.

Indian Pediatr. 2001 Oct;38(10):1148-54.

Glutaric aciduria type I misdiagnosed as Leigh's encephalopathy and cerebral palsy.

Dev Med Child Neurol. 1985 Aug;27(4):514-8. doi: 10.1111/j.1469-8749.1985.tb04576.x.

L-carnitine treatment in glutaric aciduria type I.

Neurology. 1986 Feb;36(2):264-7. doi: 10.1212/wnl.36.2.264.

Glutaric aciduria type I: clinical heterogeneity and neuroradiologic features.

Neurology. 1987 Oct;37(10):1654-7. doi: 10.1212/wnl.37.10.1654.

[Glutaric aciduria type I].

Tidsskr Nor Laegeforen. 1992 Mar 20;112(8):1020-2.

[Hyperthyroidism in early childhood and a very rare variant of glutaric aciduria: coincidence or causal relation?].

Klin Padiatr. 2001 Jan-Feb;213(1):13-6. doi: 10.1055/s-2001-11266.

引用本文的文献

Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review.

World J Pediatr. 2016 Aug;12(3):368-371. doi: 10.1007/s12519-016-0042-x. Epub 2016 Jun 29.

Rhabdomyolysis in glutaric aciduria type I.

J Inherit Metab Dis. 2003;26(7):711-2. doi: 10.1023/b:boli.0000005635.89043.8a.

本文引用的文献

Glutaric aciduria type 1 (glutaryl-CoA-dehydrogenase deficiency): advances and unanswered questions. Report from an international meeting.

Eur J Pediatr. 1997 Nov;156(11):821-8. doi: 10.1007/s004310050721.

Myoglobinuria, malignant hyperthermia, neuroleptic malignant syndrome and serotonin syndrome.

Neurol Clin. 1997 Aug;15(3):649-71. doi: 10.1016/s0733-8619(05)70338-8.

Early signs and course of disease of glutaryl-CoA dehydrogenase deficiency.

J Inherit Metab Dis. 1995;18(2):173-6. doi: 10.1007/BF00711759.