Literature DB >> 32373662

Phasic Knee Bending Dystonic and Parkinsonian Gait: A Characteristic Finding in X-Linked Dystonia Parkinsonism.

Christopher D Stephen1, Criscely L Go2, Patrick Acuna1, Nutan Sharma1.   

Abstract

BACKGROUND: X-linked dystonia parkinsonism (XDP) is a rare disorder characterized by adult-onset, progressive dystonia that, over time, is combined with or replaced by features of parkinsonism. Gait impairment is common.
METHODS: Case series of 4 XDP patients with a unique gait disorder.
RESULTS: The patients displayed a characteristic gait disorder with combined dystonic and parkinsonian gait features, with phasic knee bending. Of these patients, all had parkinsonism and three-quarters had prominent dystonic features, but 1 had predominant parkinsonism and subtle dystonic features.
CONCLUSION: Although XDP is a classic form of dystonia parkinsonism, some cases can mimic idiopathic Parkinson's disease. We describe a gait disorder which appears unique to XDP, involving phasic dystonic knee bending superimposed on parkinsonian shuffling, and may help clinically differentiate one of our parkinsonian-predominant patients from more-common forms of parkinsonism. The gait is distinct from other complex dystonic disorders with gait involvement.
© 2020 International Parkinson and Movement Disorder Society.

Entities:  

Keywords:  dystonia; dystonia parkinsonism; gait disorder; parkinsonism

Year:  2020        PMID: 32373662      PMCID: PMC7197325          DOI: 10.1002/mdc3.12929

Source DB:  PubMed          Journal:  Mov Disord Clin Pract        ISSN: 2330-1619


  9 in total

1.  Phenomenology of "Lubag" or X-linked dystonia-parkinsonism.

Authors:  Virgilio Gerald H Evidente; Joel Advincula; Raymund Esteban; Paul Pasco; Jhoe Anthony Alfon; Filipinas F Natividad; Joven Cuanang; Amado San Luis; Katrina Gwinn-Hardy; John Hardy; Dena Hernandez; Andrew Singleton
Journal:  Mov Disord       Date:  2002-11       Impact factor: 10.338

2.  Whispering dysphonia in an Australian family (DYT4): a clinical and genetic reappraisal.

Authors:  Robert A Wilcox; Susen Winkler; Katja Lohmann; Christine Klein
Journal:  Mov Disord       Date:  2011-09-28       Impact factor: 10.338

Review 3.  The unique phenomenology of sex-linked dystonia parkinsonism (XDP, DYT3, "Lubag").

Authors:  Lillian V Lee; Corazon Rivera; Rosalia A Teleg; Marita B Dantes; Paul Matthew D Pasco; Roland Dominic G Jamora; Jose Arancillo; Rodelyn F Villareal-Jordan; Raymond L Rosales; Cynthia Demaisip; Elma Maranon; Olivia Peralta; Ruth Borres; Cirnueb Tolentino; Mercy Joyce Monding; Sonia Sarcia
Journal:  Int J Neurosci       Date:  2010-11-03       Impact factor: 2.292

4.  Inherited manganism: the "cock-walk" gait and typical neuroimaging features.

Authors:  Marcela Amaral Avelino; Eduardo Ferracioli Fusão; José Luiz Pedroso; Juliana Harumi Arita; Reinaldo Teixeira Ribeiro; Ricardo Silva Pinho; Karin Tuschl; Orlando G P Barsottini; Marcelo Rodrigues Masruha
Journal:  J Neurol Sci       Date:  2014-04-04       Impact factor: 3.181

5.  Characteristic head drops and axial extension in advanced chorea-acanthocytosis.

Authors:  Susanne A Schneider; Anthony E Lang; Elena Moro; Benedikt Bader; Adrian Danek; Kailash P Bhatia
Journal:  Mov Disord       Date:  2010-07-30       Impact factor: 10.338

6.  X-linked dystonia ("Lubag") presenting predominantly with parkinsonism: a more benign phenotype?

Authors:  Virgilio Gerald H Evidente; Katrina Gwinn-Hardy; John Hardy; Dena Hernandez; Andrew Singleton
Journal:  Mov Disord       Date:  2002-01       Impact factor: 10.338

Review 7.  The natural history of sex-linked recessive dystonia parkinsonism of Panay, Philippines (XDP).

Authors:  Lillian V Lee; Elma Maranon; Cynthia Demaisip; Olivia Peralta; Ruth Borres-Icasiano; Jose Arancillo; Corazon Rivera; Edwin Munoz; Kenneth Tan; Marita T Reyes
Journal:  Parkinsonism Relat Disord       Date:  2002-10       Impact factor: 4.891

8.  Disease onset in X-linked dystonia-parkinsonism correlates with expansion of a hexameric repeat within an SVA retrotransposon in TAF1.

Authors:  D Cristopher Bragg; Kotchaphorn Mangkalaphiban; Christine A Vaine; Nichita J Kulkarni; David Shin; Rachita Yadav; Jyotsna Dhakal; Mai-Linh Ton; Anne Cheng; Christopher T Russo; Mark Ang; Patrick Acuña; Criscely Go; Taylor N Franceour; Trisha Multhaupt-Buell; Naoto Ito; Ulrich Müller; William T Hendriks; Xandra O Breakefield; Nutan Sharma; Laurie J Ozelius
Journal:  Proc Natl Acad Sci U S A       Date:  2017-12-11       Impact factor: 11.205

9.  Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia.

Authors:  Joshua Hersheson; Niccolo E Mencacci; Mary Davis; Nicola MacDonald; Daniah Trabzuni; Mina Ryten; Alan Pittman; Reema Paudel; Eleanna Kara; Katherine Fawcett; Vincent Plagnol; Kailash P Bhatia; Alan J Medlar; Horia C Stanescu; John Hardy; Robert Kleta; Nicholas W Wood; Henry Houlden
Journal:  Ann Neurol       Date:  2013-02-19       Impact factor: 10.422

  9 in total
  1 in total

Review 1.  Combined dystonias: clinical and genetic updates.

Authors:  Anne Weissbach; Gerard Saranza; Aloysius Domingo
Journal:  J Neural Transm (Vienna)       Date:  2020-10-24       Impact factor: 3.575

  1 in total

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