Literature DB >> 17870652

Rapidly progressive familial parkinsonism with central hypoventilation, depression and weight loss (Perry syndrome)--a literature review.

Christian Wider1, Zbigniew K Wszolek.   

Abstract

Autosomal dominant parkinsonism, hypoventilation, depression and weight loss (Perry syndrome) has been reported in only seven families worldwide. It is a rapidly progressive disease leading to death from respiratory insufficiency within a few years. Parkinsonism is usually mild, with bradykinesia, rigidity, rest and postural tremor, and axial signs. Response to levodopa is poor although transient response has been occasionally observed. The early signs include parkinsonism, depression and weight loss, whereas hypoventilation is a late feature. Neuropathology shows severe neuronal loss in the substantia nigra, less prominent neuronal loss in the locus coeruleus, and no or few Lewy bodies. In this review, we also propose diagnostic criteria for this condition.

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Year:  2007        PMID: 17870652     DOI: 10.1016/j.parkreldis.2007.07.014

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  24 in total

Review 1.  Update on genetics of parkinsonism.

Authors:  Shinsuke Fujioka; Zbigniew K Wszolek
Journal:  Neurodegener Dis       Date:  2012-01-17       Impact factor: 2.977

Review 2.  DCTN1-related neurodegeneration: Perry syndrome and beyond.

Authors:  Takuya Konno; Owen A Ross; Hélio A G Teive; Jarosław Sławek; Dennis W Dickson; Zbigniew K Wszolek
Journal:  Parkinsonism Relat Disord       Date:  2017-06-12       Impact factor: 4.891

3.  Central hypoventilation in progressive supranuclear palsy.

Authors:  Kory S Herrick; Randy Woltjer; Thao Pham; Megan Chalupsky; Amie L Hiller
Journal:  Mov Disord Clin Pract       Date:  2016-05-19

4.  Dynactin is required for transport initiation from the distal axon.

Authors:  Armen J Moughamian; Erika L F Holzbaur
Journal:  Neuron       Date:  2012-04-26       Impact factor: 17.173

5.  α-Tubulin Tyrosination and CLIP-170 Phosphorylation Regulate the Initiation of Dynein-Driven Transport in Neurons.

Authors:  Jeffrey J Nirschl; Maria M Magiera; Jacob E Lazarus; Carsten Janke; Erika L F Holzbaur
Journal:  Cell Rep       Date:  2016-03-10       Impact factor: 9.423

6.  Elucidating the genetics and pathology of Perry syndrome.

Authors:  Christian Wider; Justus C Dachsel; Matthew J Farrer; Dennis W Dickson; Yoshio Tsuboi; Zbigniew K Wszolek
Journal:  J Neurol Sci       Date:  2009-09-04       Impact factor: 3.181

7.  DCTN1 mutation analysis in families with progressive supranuclear palsy-like phenotypes.

Authors:  Paola Caroppo; Isabelle Le Ber; Fabienne Clot; Sophie Rivaud-Péchoux; Agnès Camuzat; Anne De Septenville; Claire Boutoleau-Bretonnière; Vanessa Mourlon; Mathilde Sauvée; Thibaud Lebouvier; Anne-Marie Bonnet; Richard Levy; Martine Vercelletto; Alexis Brice
Journal:  JAMA Neurol       Date:  2014-02       Impact factor: 18.302

8.  Characterization of DCTN1 genetic variability in neurodegeneration.

Authors:  C Vilariño-Güell; C Wider; A I Soto-Ortolaza; S A Cobb; J M Kachergus; B H Keeling; J C Dachsel; M M Hulihan; D W Dickson; Z K Wszolek; R J Uitti; N R Graff-Radford; B F Boeve; K A Josephs; B Miller; K B Boylan; K Gwinn; C H Adler; J O Aasly; F Hentati; A Destée; A Krygowska-Wajs; M-C Chartier-Harlin; O A Ross; R Rademakers; M J Farrer
Journal:  Neurology       Date:  2009-06-09       Impact factor: 9.910

9.  Pallidonigral TDP-43 pathology in Perry syndrome.

Authors:  Christian Wider; Dennis W Dickson; A Jon Stoessl; Yoshio Tsuboi; Françoise Chapon; Ludwig Gutmann; Bernard Lechevalier; Donald B Calne; David A Personett; Mary Hulihan; Jennifer Kachergus; Rosa Rademakers; Matthew C Baker; Linda L Grantier; O K Sujith; Laura Brown; Susan Calne; Matthew J Farrer; Zbigniew K Wszolek
Journal:  Parkinsonism Relat Disord       Date:  2008-08-23       Impact factor: 4.891

10.  DCTN1 mutations in Perry syndrome.

Authors:  Matthew J Farrer; Mary M Hulihan; Jennifer M Kachergus; Justus C Dächsel; A Jon Stoessl; Linda L Grantier; Susan Calne; Donald B Calne; Bernard Lechevalier; Francoise Chapon; Yoshio Tsuboi; Tatsuo Yamada; Ludwig Gutmann; Bülent Elibol; Kailash P Bhatia; Christian Wider; Carles Vilariño-Güell; Owen A Ross; Laura A Brown; Monica Castanedes-Casey; Dennis W Dickson; Zbigniew K Wszolek
Journal:  Nat Genet       Date:  2009-01-11       Impact factor: 38.330

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