Literature DB >> 18570303

Characterization of PLA2G6 as a locus for dystonia-parkinsonism.

Coro Paisan-Ruiz1, Kailash P Bhatia, Abi Li, Dena Hernandez, Mary Davis, Nick W Wood, John Hardy, Henry Houlden, Andrew Singleton, Susanne A Schneider.   

Abstract

BACKGROUND: Although many recessive loci causing parkinsonism dystonia have been identified, these do not explain all cases of the disorder.
METHODS: We used homozygosity mapping and mutational analysis in three individuals from two unrelated families who presented with adult-onset levodopa-responsive dystonia-parkinsonism, pyramidal signs and cognitive/psychiatric features, and cerebral and cerebellar atrophy on magnetic resonance imaging but absent iron in the basal ganglia.
RESULTS: We identified areas of homozygosity on chromosome 22 and, subsequently, PLA2G6 mutations.
INTERPRETATION: PLA2G6 mutations are associated with infantile neuroaxonal dystrophy and have been reported previously to cause early cerebellar signs, and the syndrome was classified as neurodegeneration with brain iron accumulation (type 2). Our cases have neither of these previously pathognomic features. Thus, mutations in PLA2G6 should additionally be considered in patients with adult-onset dystonia-parkinsonism even with absent iron on brain imaging.

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Year:  2009        PMID: 18570303      PMCID: PMC9016626          DOI: 10.1002/ana.21415

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   11.274


  15 in total

1.  Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria.

Authors:  N Nardocci; G Zorzi; L Farina; S Binelli; W Scaioli; C Ciano; L Verga; L Angelini; M Savoiardo; O Bugiani
Journal:  Neurology       Date:  1999-04-22       Impact factor: 9.910

2.  A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome.

Authors:  B Zhou; S K Westaway; B Levinson; M A Johnson; J Gitschier; S J Hayflick
Journal:  Nat Genet       Date:  2001-08       Impact factor: 38.330

3.  Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.

Authors:  Alfredo Ramirez; André Heimbach; Jan Gründemann; Barbara Stiller; Dan Hampshire; L Pablo Cid; Ingrid Goebel; Ammar F Mubaidin; Abdul-Latif Wriekat; Jochen Roeper; Amir Al-Din; Axel M Hillmer; Meliha Karsak; Birgit Liss; C Geoffrey Woods; Maria I Behrens; Christian Kubisch
Journal:  Nat Genet       Date:  2006-09-10       Impact factor: 38.330

4.  PLA2G6 mutation underlies infantile neuroaxonal dystrophy.

Authors:  Shareef Khateeb; Hagit Flusser; Rivka Ofir; Ilan Shelef; Ginat Narkis; Gideon Vardi; Zamir Shorer; Rachel Levy; Aharon Galil; Khalil Elbedour; Ohad S Birk
Journal:  Am J Hum Genet       Date:  2006-09-19       Impact factor: 11.025

5.  Severe tongue protrusion dystonia: clinical syndromes and possible treatment.

Authors:  S A Schneider; A Aggarwal; M Bhatt; E Dupont; S Tisch; P Limousin; P Lee; N Quinn; K P Bhatia
Journal:  Neurology       Date:  2006-09-26       Impact factor: 9.910

6.  Kufor Rakeb disease: autosomal recessive, levodopa-responsive parkinsonism with pyramidal degeneration, supranuclear gaze palsy, and dementia.

Authors:  David R Williams; Ali Hadeed; Amir S Najim al-Din; Abdel-Latif Wreikat; Andrew J Lees
Journal:  Mov Disord       Date:  2005-10       Impact factor: 10.338

7.  Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.

Authors:  Vincenzo Bonifati; Patrizia Rizzu; Marijke J van Baren; Onno Schaap; Guido J Breedveld; Elmar Krieger; Marieke C J Dekker; Ferdinando Squitieri; Pablo Ibanez; Marijke Joosse; Jeroen W van Dongen; Nicola Vanacore; John C van Swieten; Alexis Brice; Giuseppe Meco; Cornelia M van Duijn; Ben A Oostra; Peter Heutink
Journal:  Science       Date:  2002-11-21       Impact factor: 47.728

8.  Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN).

Authors:  M A Kurian; N V Morgan; L MacPherson; K Foster; D Peake; R Gupta; S G Philip; C Hendriksz; J E V Morton; H M Kingston; E M Rosser; E Wassmer; P Gissen; E R Maher
Journal:  Neurology       Date:  2008-04-29       Impact factor: 9.910

9.  DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA.

Authors:  Sarah Camargos; Sonja Scholz; Javier Simón-Sánchez; Coro Paisán-Ruiz; Patrick Lewis; Dena Hernandez; Jinhui Ding; J Raphael Gibbs; Mark R Cookson; Jose Bras; Rita Guerreiro; Catarina Resende Oliveira; Andrew Lees; John Hardy; Francisco Cardoso; Andrew B Singleton
Journal:  Lancet Neurol       Date:  2008-02-01       Impact factor: 44.182

10.  PINK1 mutations are associated with sporadic early-onset parkinsonism.

Authors:  Enza Maria Valente; Sergio Salvi; Tamara Ialongo; Roberta Marongiu; Antonio Emanuele Elia; Viviana Caputo; Luigi Romito; Alberto Albanese; Bruno Dallapiccola; Anna Rita Bentivoglio
Journal:  Ann Neurol       Date:  2004-09       Impact factor: 10.422

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  137 in total

1.  Identification of Novel Compound Mutations in PLA2G6-Associated Neurodegeneration Patient with Characteristic MRI Imaging.

Authors:  Sen Guo; Liu Yang; Huijie Liu; Wei Chen; Jinchen Li; Ping Yu; Zhong Sheng Sun; Xiang Chen; Jie Du; Tao Cai
Journal:  Mol Neurobiol       Date:  2016-07-09       Impact factor: 5.590

Review 2.  Genetics of neurodegeneration with brain iron accumulation.

Authors:  Allison Gregory; Susan J Hayflick
Journal:  Curr Neurol Neurosci Rep       Date:  2011-06       Impact factor: 5.081

Review 3.  Pantothenate kinase-associated neurodegeneration (PKAN) and PLA2G6-associated neurodegeneration (PLAN): review of two major neurodegeneration with brain iron accumulation (NBIA) phenotypes.

Authors:  Manju A Kurian; Susan J Hayflick
Journal:  Int Rev Neurobiol       Date:  2013       Impact factor: 3.230

Review 4.  The neuropathology of neurodegeneration with brain iron accumulation.

Authors:  Michael C Kruer
Journal:  Int Rev Neurobiol       Date:  2013       Impact factor: 3.230

5.  Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia.

Authors:  A Deik; B Johannes; J C Rucker; E Sánchez; S E Brodie; E Deegan; K Landy; Y Kajiwara; S Scelsa; R Saunders-Pullman; C Paisán-Ruiz
Journal:  J Neurol       Date:  2014-09-30       Impact factor: 4.849

Review 6.  The genetics of Parkinson's disease: progress and therapeutic implications.

Authors:  Andrew B Singleton; Matthew J Farrer; Vincenzo Bonifati
Journal:  Mov Disord       Date:  2013-01       Impact factor: 10.338

Review 7.  Current perspective of mitochondrial biology in Parkinson's disease.

Authors:  Navneet Ammal Kaidery; Bobby Thomas
Journal:  Neurochem Int       Date:  2018-03-14       Impact factor: 3.921

8.  PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism.

Authors:  Hamidreza Khodadadi; Luis J Azcona; Vajiheh Aghamollaii; Mir Davood Omrani; Masoud Garshasbi; Shaghayegh Taghavi; Abbas Tafakhori; Gholam Ali Shahidi; Javad Jamshidi; Hossein Darvish; Coro Paisán-Ruiz
Journal:  Mov Disord       Date:  2016-10-18       Impact factor: 10.338

9.  Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations.

Authors:  Eng-King Tan; Chin-Hslen Lin; Chun-Hwei Tai; Louis C Tan; Meng-Ling Chen; R Li; Hui-Qin Lim; Ratnagopal Pavanni; Yih Yuen; K M Prakash; Yi Zhao; Ruey-Meei Wu
Journal:  Hum Genet       Date:  2009-05-16       Impact factor: 4.132

Review 10.  Clinical and genetic delineation of neurodegeneration with brain iron accumulation.

Authors:  A Gregory; B J Polster; S J Hayflick
Journal:  J Med Genet       Date:  2008-11-03       Impact factor: 6.318

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