Review
[Hereditary metabolic causes of stroke and pseudo-stroke in adulthood]
[Article in
French]
Affiliations
- PMID: 11794878
Item in Clipboard
Review
[Hereditary metabolic causes of stroke and pseudo-stroke in adulthood]
[Article in
French]
Rev Med Interne.
2001 Dec.
Abstract
Metabolic diseases are a rare cause of strokes. However, prevention and treatment are available for some of them. This work describes some metabolic diseases generating strokes by disturbing directly vascular function (homocysteine disorders, Fabry disease, congenital defects of glycosylation) and those for which clinical presentation is similar to a stroke (urea cycle disorders, branched-chain organic acidurias, mitochondrial diseases).
Similar articles
-
Inherited metabolic disorders and stroke part 2: homocystinuria, organic acidurias, and urea cycle disorders.Arch Neurol. 2010 Feb;67(2):148-53. doi: 10.1001/archneurol.2009.333. Arch Neurol. 2010. PMID: 20142522 Review.
-
Homocysteinemia: association of a metabolic disorder with vascular disease and thrombosis.Thromb Res. 1993 Sep 1;71(5):337-59. doi: 10.1016/0049-3848(93)90160-p. Thromb Res. 1993. PMID: 8236162 Review. No abstract available.
-
Methylenetetrahydrofolate reductase deficiency in a patient with phenotypic findings of Angelman syndrome.Am J Med Genet. 1998 May 18;77(3):198-200. Am J Med Genet. 1998. PMID: 9605586
-
Stroke and stroke-like episodes in inborn errors of metabolism: Pathophysiological and clinical implications.Mol Genet Metab. 2022 Jan;135(1):3-14. doi: 10.1016/j.ymgme.2021.12.014. Epub 2021 Dec 23. Mol Genet Metab. 2022. PMID: 34996714 Review.
-
Intermittent encephalopathy, reversible nerve conduction slowing, and MRI evidence of cerebral white matter disease in methylenetetrahydrofolate reductase deficiency.Neurology. 1994 Feb;44(2):344-7. doi: 10.1212/wnl.44.2.344. Neurology. 1994. PMID: 8309589
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical