2014
DOI: 10.1111/ane.12231
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Dystonia - new advances in classification, genetics, pathophysiology and treatment

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Cited by 42 publications
(23 citation statements)
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“…Moreover, it has been proposed to designate GCH1deficiency and THD as 'dystonia 5a' and 'dystonia 5b' [2,3].Tyrosine hydroxylase deficiency (OMIM191290) is a rare cause of autosomal recessive DRD due to mutations in TH on chromosome 11p15.5.The enzyme tyrosine hydroxylase (EC 1.14.16.2) catalyzes the conversion of L-tyrosine to L-dopa, which is the rate-limiting step in the biosynthesis of the catecholamine's.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, it has been proposed to designate GCH1deficiency and THD as 'dystonia 5a' and 'dystonia 5b' [2,3].Tyrosine hydroxylase deficiency (OMIM191290) is a rare cause of autosomal recessive DRD due to mutations in TH on chromosome 11p15.5.The enzyme tyrosine hydroxylase (EC 1.14.16.2) catalyzes the conversion of L-tyrosine to L-dopa, which is the rate-limiting step in the biosynthesis of the catecholamine's.…”
Section: Discussionmentioning
confidence: 99%
“…[1][2][3][4][5][6][7][10][11] There are many forms of Paroxysmal Dystonia/Dyskinesia, but there are only a few that are ever diagnosed which are Paroxysmal Kinesigenic Dystonia (PKD), Paroxysmal Non-kinesigenic Dystonia (PNKD), and Paroxysmal Exercise-induced Dystonia (PED). The most common out of the three is PKD.…”
Section: Related Literaturementioning
confidence: 99%
“…Focal hand dystonia in musicians is one of the major types of dystonia that has received a vast attention over period of time. 2 Focal hand dystonia which develops secondary to some condition like stroke, Parkinsonism or brain injury is although very devastating but still ignored.…”
Section: Introductionmentioning
confidence: 99%