Literature DB >> 4082906

A survival analysis of 155 cases of progressive muscular atrophy.

A Chiò, F Brignolio, M Leone, P Mortara, M G Rosso, A Tribolo, D Schiffer.   

Abstract

We performed a survival analysis of 155 cases of progressive muscular atrophy (PMA). In about half the cases, hands were involved first, the lower limbs in 30% and the shoulder girdle in 23%. The lifetables of PMA, adjusted to the expected mortality, showed a survival rate of 61.3% and 56.4% at three and five years, respectively. The location of onset symptoms did not modify the life expectancy, whereas the age of the patients at the moment of first diagnosis had a great influence on the course of the disease. The patients were further subdivided in two groups on the basis of the diffusion of the neuromuscular damage at the moment of the diagnosis. The course of the patients with a localized disease was markedly better than that of subjects with widespread disease. Some hypotheses are made about the latter group of cases.

Entities:  

Mesh:

Year:  1985        PMID: 4082906     DOI: 10.1111/j.1600-0404.1985.tb00892.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  8 in total

Review 1.  [Progressive muscle atrophy. A rarely diagnosed variant of amyotrophic lateral sclerosis].

Authors:  T Meyer; C Münch; F K H van Landeghem; N Borisow; J Dullinger; P Linke
Journal:  Nervenarzt       Date:  2007-12       Impact factor: 1.214

2.  Atypical form of amyotrophic lateral sclerosis.

Authors:  S Sasaki; M Iwata
Journal:  J Neurol Neurosurg Psychiatry       Date:  1999-05       Impact factor: 10.154

3.  A follow-up study of 60 cases of chronic spinal muscular atrophy.

Authors:  D Schiffer; F Brignolio; A Chiò; M T Giordana; P Meineri; M G Rosso; A Tribolo
Journal:  Ital J Neurol Sci       Date:  1988-02

4.  The prognosis of adult-onset motor neuron disease: a prospective study based on the Scottish Motor Neuron Disease Register.

Authors:  A M Chancellor; J M Slattery; H Fraser; R J Swingler; S M Holloway; C P Warlow
Journal:  J Neurol       Date:  1993-06       Impact factor: 4.849

Review 5.  Prognostic factors in ALS: A critical review.

Authors:  Adriano Chiò; Giancarlo Logroscino; Orla Hardiman; Robert Swingler; Douglas Mitchell; Ettore Beghi; Bryan G Traynor
Journal:  Amyotroph Lateral Scler       Date:  2009 Oct-Dec

6.  Study of 962 patients indicates progressive muscular atrophy is a form of ALS.

Authors:  W-K Kim; X Liu; J Sandner; M Pasmantier; J Andrews; L P Rowland; H Mitsumoto
Journal:  Neurology       Date:  2009-11-17       Impact factor: 9.910

7.  [Calculation of the prevalence of progressive muscular atrophy among adults in China based on urban medical insurance data from 15 provinces].

Authors:  L Xu; L Chen; D S Fan; J N Feng; L L Liu; S Y Zhan; S F Wang
Journal:  Beijing Da Xue Xue Bao Yi Xue Ban       Date:  2020-06-18

8.  Natural history and clinical features of the flail arm and flail leg ALS variants.

Authors:  L C Wijesekera; S Mathers; P Talman; C Galtrey; M H Parkinson; J Ganesalingam; E Willey; M A Ampong; C M Ellis; C E Shaw; A Al-Chalabi; P N Leigh
Journal:  Neurology       Date:  2009-03-24       Impact factor: 9.910

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.