Literature DB >> 31187296

Paroxysmal Movement Disorders: Recent Advances.

Zheyu Xu1, Che-Kang Lim2,3, Louis C S Tan1,4, Eng-King Tan5,6.   

Abstract

PURPOSE OF REVIEW: Recent advancements in next-generation sequencing (NGS) have enabled techniques such as whole exome sequencing (WES) and whole genome sequencing (WGS) to be used to study paroxysmal movement disorders (PMDs). This review summarizes how the recent genetic advances have altered our understanding of the pathophysiology and treatment of the PMDs. Recently described disease entities are also discussed. RECENT
FINDINGS: With the recognition of the phenotypic and genotypic heterogeneity that occurs amongst the PMDs, an increasing number of gene mutations are now implicated to cause the disorders. PMDs can also occur as part of a complex phenotype. The increasing complexity of PMDs challenges the way we view and classify them. The identification of new causative genes and their genotype-phenotype correlation will shed more light on the underlying pathophysiology and will facilitate development of genetic testing guidelines and identification of novel drug targets for PMDs.

Entities:  

Keywords:  Episodic ataxia (EA); Genetics; Paroxysmal exercise-induced dyskinesia (PED); Paroxysmal kinesigenic dyskinesia (PKD); Paroxysmal non-kinesigenic dyskinesia (PNKD)

Mesh:

Substances:

Year:  2019        PMID: 31187296     DOI: 10.1007/s11910-019-0958-3

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  111 in total

1.  Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures.

Authors:  J C Jen; J Wan; T P Palos; B D Howard; R W Baloh
Journal:  Neurology       Date:  2005-08-23       Impact factor: 9.910

2.  Clinical and genetic spectrum of pyruvate dehydrogenase deficiency: dihydrolipoamide acetyltransferase (E2) deficiency.

Authors:  Rosemary A Head; Ruth M Brown; Zarazuela Zolkipli; Raveen Shahdadpuri; Mary D King; Peter T Clayton; Garry K Brown
Journal:  Ann Neurol       Date:  2005-08       Impact factor: 10.422

3.  A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.

Authors:  M Z Cader; J L Steckley; D A Dyment; R S McLachlan; G C Ebers
Journal:  Neurology       Date:  2005-07-12       Impact factor: 9.910

4.  Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1.

Authors:  H a Tomita; S Nagamitsu; K Wakui; Y Fukushima; K Yamada; M Sadamatsu; A Masui; T Konishi; T Matsuishi; M Aihara; K Shimizu; K Hashimoto; M Mineta; M Matsushima; T Tsujita; M Saito; H Tanaka; S Tsuji; T Takagi; Y Nakamura; S Nanko; N Kato; Y Nakane; N Niikawa
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

5.  Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene.

Authors:  Charles E Schwartz; Melanie M May; Nancy J Carpenter; R Curtis Rogers; Judith Martin; Martin G Bialer; Jewell Ward; Javier Sanabria; Silvana Marsa; James A Lewis; Roberto Echeverri; Herbert A Lubs; Kytja Voeller; Richard J Simensen; Roger E Stevenson
Journal:  Am J Hum Genet       Date:  2005-05-11       Impact factor: 11.025

6.  Piracetam and levetiracetam, two pyrrolidone derivatives, exert antidystonic activity in a hamster model of paroxysmal dystonia.

Authors:  W Löscher; A Richter
Journal:  Eur J Pharmacol       Date:  2000-03-17       Impact factor: 4.432

7.  Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.

Authors:  A Escayg; M De Waard; D D Lee; D Bichet; P Wolf; T Mayer; J Johnston; R Baloh; T Sander; M H Meisler
Journal:  Am J Hum Genet       Date:  2000-04-04       Impact factor: 11.025

8.  Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis.

Authors:  Shirley Rainier; Donald Thomas; Debra Tokarz; Lei Ming; Melanie Bui; Erin Plein; Xinping Zhao; Rosemary Lemons; Roger Albin; Colin Delaney; David Alvarado; John K Fink
Journal:  Arch Neurol       Date:  2004-07

9.  A new Chrna4 mutation with low penetrance in nocturnal frontal lobe epilepsy.

Authors:  Tobias Leniger; Colette Kananura; Andreas Hufnagel; Sonia Bertrand; Daniel Bertrand; Ortrud K Steinlein
Journal:  Epilepsia       Date:  2003-07       Impact factor: 5.864

10.  A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1.

Authors:  A Gambardella; G Annesi; M De Fusco; A Patrignani; U Aguglia; F Annesi; A A Pasqua; P Spadafora; R L Oliveri; P Valentino; M Zappia; A Ballabio; G Casari; A Quattrone
Journal:  Neurology       Date:  2000-11-28       Impact factor: 9.910

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  3 in total

1.  Mitochondrial PCK2 Missense Variant in Shetland Sheepdogs with Paroxysmal Exercise-Induced Dyskinesia (PED).

Authors:  Jasmin Nessler; Petra Hug; Paul J J Mandigers; Peter A J Leegwater; Vidhya Jagannathan; Anibh M Das; Marco Rosati; Kaspar Matiasek; Adrian C Sewell; Marion Kornberg; Marina Hoffmann; Petra Wolf; Andrea Fischer; Andrea Tipold; Tosso Leeb
Journal:  Genes (Basel)       Date:  2020-07-09       Impact factor: 4.096

2.  Paroxysmal kinesigenic dyskinesia associated with a novel POLG variant: A case report.

Authors:  Yaping Zhou; Jian Zhang; Xiaoting Wang; Qian Peng; Xiuli Shang
Journal:  Medicine (Baltimore)       Date:  2021-01-29       Impact factor: 1.817

Review 3.  Paroxysmal Movement Disorders.

Authors:  Susan Harvey; Mary D King; Kathleen M Gorman
Journal:  Front Neurol       Date:  2021-06-11       Impact factor: 4.003

  3 in total

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