Motor neuron diseases in the University Hospital of Fortaleza (Northeastern Brazil): a clinico-demographic analysis of 87 cases

In this retrospective (1980-1998) study, we have analyzed clinico-demographically, from the records of the University Hospital of Fortaleza (Brazil), a group of 87 patients showing signs and symptoms of motor neuron diseases (MNDs). Their diagnosis was determined clinically and laboratorially. The W...

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Main Authors: CARLOS M. DE CASTRO-COSTA, REINALDO B. ORIÁ, OTONI C. DO VALE, JOSÉ ARNALDO M. DE ARRUDA, WAGNER G. HORTA, JOSÉ ARTUR C. D'ALMEIDA, TEREZINHA J.T. SANTOS, RODRIGO S.N. RAMOS, MARCUS A.C. GIFONI
Format: Article
Language:English
Published: Academia Brasileira de Neurologia (ABNEURO) 2000-12-01
Series:Arquivos de Neuro-Psiquiatria
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2000000600002&tlng=en
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author CARLOS M. DE CASTRO-COSTA
REINALDO B. ORIÁ
OTONI C. DO VALE
JOSÉ ARNALDO M. DE ARRUDA
WAGNER G. HORTA
JOSÉ ARTUR C. D'ALMEIDA
TEREZINHA J.T. SANTOS
RODRIGO S.N. RAMOS
MARCUS A.C. GIFONI
author_facet CARLOS M. DE CASTRO-COSTA
REINALDO B. ORIÁ
OTONI C. DO VALE
JOSÉ ARNALDO M. DE ARRUDA
WAGNER G. HORTA
JOSÉ ARTUR C. D'ALMEIDA
TEREZINHA J.T. SANTOS
RODRIGO S.N. RAMOS
MARCUS A.C. GIFONI
author_sort CARLOS M. DE CASTRO-COSTA
collection DOAJ
description In this retrospective (1980-1998) study, we have analyzed clinico-demographically, from the records of the University Hospital of Fortaleza (Brazil), a group of 87 patients showing signs and symptoms of motor neuron diseases (MNDs). Their diagnosis was determined clinically and laboratorially. The WFN criteria were used for amyotrophic lateral sclerosis (ALS) diagnosis. The clinico-demographic analysis of the 87 cases of MNDs showed that 4 were diagnosed as spinal muscular atrophy (SMA), 5 cases as ALS subsets: 2 as progressive bulbar paralysis (PBP), 2 as progressive muscular atrophy (PMA) and 1 as monomelic amyotrophy (MA), and 78 cases of ALS. The latter comprised 51 males and 27 females, with a mean age of 42.02 years. They were sub-divided into 4 groups according to age: from 15 to 29 years (n= 17), 30 to 39 years (n= 18), 40 to 69 years (n= 39) and 70 to 78 years (n= 4). From the 78 ALS patients, 76 were of the classic sporadic form whilst only 2 were of the familial form. The analysis of the 87 patients with MNDs from the University Hospital of Fortaleza showed a predominance of ALS patients, with a high number of cases of juvenile and early onset adult sporadic ALS.
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spelling doaj.art-f256cb1326ba4c24af2393b503882f192022-12-21T21:34:17ZengAcademia Brasileira de Neurologia (ABNEURO)Arquivos de Neuro-Psiquiatria1678-42272000-12-01584986989Motor neuron diseases in the University Hospital of Fortaleza (Northeastern Brazil): a clinico-demographic analysis of 87 casesCARLOS M. DE CASTRO-COSTA0REINALDO B. ORIÁ1OTONI C. DO VALE2JOSÉ ARNALDO M. DE ARRUDA3WAGNER G. HORTA4JOSÉ ARTUR C. D'ALMEIDA5TEREZINHA J.T. SANTOS6RODRIGO S.N. RAMOS7MARCUS A.C. GIFONI8Federal University of CearáFederal University of CearáFederal University of CearáFederal University of CearáFederal University of CearáFederal University of CearáFederal University of CearáFederal University of CearáFederal University of CearáIn this retrospective (1980-1998) study, we have analyzed clinico-demographically, from the records of the University Hospital of Fortaleza (Brazil), a group of 87 patients showing signs and symptoms of motor neuron diseases (MNDs). Their diagnosis was determined clinically and laboratorially. The WFN criteria were used for amyotrophic lateral sclerosis (ALS) diagnosis. The clinico-demographic analysis of the 87 cases of MNDs showed that 4 were diagnosed as spinal muscular atrophy (SMA), 5 cases as ALS subsets: 2 as progressive bulbar paralysis (PBP), 2 as progressive muscular atrophy (PMA) and 1 as monomelic amyotrophy (MA), and 78 cases of ALS. The latter comprised 51 males and 27 females, with a mean age of 42.02 years. They were sub-divided into 4 groups according to age: from 15 to 29 years (n= 17), 30 to 39 years (n= 18), 40 to 69 years (n= 39) and 70 to 78 years (n= 4). From the 78 ALS patients, 76 were of the classic sporadic form whilst only 2 were of the familial form. The analysis of the 87 patients with MNDs from the University Hospital of Fortaleza showed a predominance of ALS patients, with a high number of cases of juvenile and early onset adult sporadic ALS.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2000000600002&tlng=enmotor neuron diseasesamyotrophic lateral sclerosisFortaleza (Brazil)
spellingShingle CARLOS M. DE CASTRO-COSTA
REINALDO B. ORIÁ
OTONI C. DO VALE
JOSÉ ARNALDO M. DE ARRUDA
WAGNER G. HORTA
JOSÉ ARTUR C. D'ALMEIDA
TEREZINHA J.T. SANTOS
RODRIGO S.N. RAMOS
MARCUS A.C. GIFONI
Motor neuron diseases in the University Hospital of Fortaleza (Northeastern Brazil): a clinico-demographic analysis of 87 cases
Arquivos de Neuro-Psiquiatria
motor neuron diseases
amyotrophic lateral sclerosis
Fortaleza (Brazil)
title Motor neuron diseases in the University Hospital of Fortaleza (Northeastern Brazil): a clinico-demographic analysis of 87 cases
title_full Motor neuron diseases in the University Hospital of Fortaleza (Northeastern Brazil): a clinico-demographic analysis of 87 cases
title_fullStr Motor neuron diseases in the University Hospital of Fortaleza (Northeastern Brazil): a clinico-demographic analysis of 87 cases
title_full_unstemmed Motor neuron diseases in the University Hospital of Fortaleza (Northeastern Brazil): a clinico-demographic analysis of 87 cases
title_short Motor neuron diseases in the University Hospital of Fortaleza (Northeastern Brazil): a clinico-demographic analysis of 87 cases
title_sort motor neuron diseases in the university hospital of fortaleza northeastern brazil a clinico demographic analysis of 87 cases
topic motor neuron diseases
amyotrophic lateral sclerosis
Fortaleza (Brazil)
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2000000600002&tlng=en
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