X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIES

Detalhes bibliográficos
Autor(a) principal: Furlan,Fernanda Luiza Schumacher
Data de Publicação: 2019
Outros Autores: Lemes,Macleise Andres, Suguimatsu,Ligia Cecilia Fuverki, Pires,Carolina Teixeira Furquim, Santos,Mara Lucia Schmitz Ferreira
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista Paulista de Pediatria (Ed. Português. Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822019000400465
Resumo: ABSTRACT Objective: To describe patients with different phenotypes of X-linked adrenoleukodystrophy: pre-symptomatic, cerebral demyelinating inflammatory adrenoleukodystrophy, adrenomyeloneuropathy and adrenal insufficiency only. Methods: Specific data related to epidemiology, phenotype, diagnosis and treatment of 24 patients with X-linked adrenoleukodystrophy were collected. A qualitative cross-sectional and descriptive-exploratory analysis was performed using medical records from a reference center in Neuropediatrics in Curitiba, Brazil, as well as an electronic questionnaire. Results: The majority (79%) of patients had cerebral demyelinating inflammatory adrenoleukodystrophy, presenting aphasia, hyperactivity and vision disorders as the main initial symptoms. These symptoms appeared, on average, between six and seven years of age. There was a mean delay of 11 months between the onset of symptoms/signs and the diagnosis. Patients sought diagnosis mainly with neuropediatricians, and the main requested tests were dosage of very long chain fatty acids and brain magnetic resonance. Conclusions: All phenotypes of X-linked adrenoleukodystrophy, except for myelopathy in women, were presented in the studied population, which mainly consisted of children and adolescents. Prevalent signs and symptoms registered in the literature were observed. Most of the patients with cerebral demyelinating inflammatory adrenoleukodystrophy were not diagnosed in time for hematopoietic stem cell transplantation.
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spelling X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIESAdrenoleukodystrophyPeroxisomal disordersDemyelinating diseasesBone marrow transplantationAphasiaAdrenal insufficiencyABSTRACT Objective: To describe patients with different phenotypes of X-linked adrenoleukodystrophy: pre-symptomatic, cerebral demyelinating inflammatory adrenoleukodystrophy, adrenomyeloneuropathy and adrenal insufficiency only. Methods: Specific data related to epidemiology, phenotype, diagnosis and treatment of 24 patients with X-linked adrenoleukodystrophy were collected. A qualitative cross-sectional and descriptive-exploratory analysis was performed using medical records from a reference center in Neuropediatrics in Curitiba, Brazil, as well as an electronic questionnaire. Results: The majority (79%) of patients had cerebral demyelinating inflammatory adrenoleukodystrophy, presenting aphasia, hyperactivity and vision disorders as the main initial symptoms. These symptoms appeared, on average, between six and seven years of age. There was a mean delay of 11 months between the onset of symptoms/signs and the diagnosis. Patients sought diagnosis mainly with neuropediatricians, and the main requested tests were dosage of very long chain fatty acids and brain magnetic resonance. Conclusions: All phenotypes of X-linked adrenoleukodystrophy, except for myelopathy in women, were presented in the studied population, which mainly consisted of children and adolescents. Prevalent signs and symptoms registered in the literature were observed. Most of the patients with cerebral demyelinating inflammatory adrenoleukodystrophy were not diagnosed in time for hematopoietic stem cell transplantation.Sociedade de Pediatria de São Paulo2019-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822019000400465Revista Paulista de Pediatria v.37 n.4 2019reponame:Revista Paulista de Pediatria (Ed. Português. Online)instname:Sociedade de Pediatria de São Paulo (SPSP)instacron:SPSP10.1590/1984-0462/;2019;37;4;00015info:eu-repo/semantics/openAccessFurlan,Fernanda Luiza SchumacherLemes,Macleise AndresSuguimatsu,Ligia Cecilia FuverkiPires,Carolina Teixeira FurquimSantos,Mara Lucia Schmitz Ferreiraeng2019-10-07T00:00:00Zoai:scielo:S0103-05822019000400465Revistahttps://www.rpped.com.br/ONGhttps://old.scielo.br/oai/scielo-oai.phppediatria@spsp.org.br||rpp@spsp.org.br1984-04620103-0582opendoar:2019-10-07T00:00Revista Paulista de Pediatria (Ed. Português. Online) - Sociedade de Pediatria de São Paulo (SPSP)false
dc.title.none.fl_str_mv X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIES
title X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIES
spellingShingle X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIES
Furlan,Fernanda Luiza Schumacher
Adrenoleukodystrophy
Peroxisomal disorders
Demyelinating diseases
Bone marrow transplantation
Aphasia
Adrenal insufficiency
title_short X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIES
title_full X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIES
title_fullStr X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIES
title_full_unstemmed X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIES
title_sort X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIES
author Furlan,Fernanda Luiza Schumacher
author_facet Furlan,Fernanda Luiza Schumacher
Lemes,Macleise Andres
Suguimatsu,Ligia Cecilia Fuverki
Pires,Carolina Teixeira Furquim
Santos,Mara Lucia Schmitz Ferreira
author_role author
author2 Lemes,Macleise Andres
Suguimatsu,Ligia Cecilia Fuverki
Pires,Carolina Teixeira Furquim
Santos,Mara Lucia Schmitz Ferreira
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Furlan,Fernanda Luiza Schumacher
Lemes,Macleise Andres
Suguimatsu,Ligia Cecilia Fuverki
Pires,Carolina Teixeira Furquim
Santos,Mara Lucia Schmitz Ferreira
dc.subject.por.fl_str_mv Adrenoleukodystrophy
Peroxisomal disorders
Demyelinating diseases
Bone marrow transplantation
Aphasia
Adrenal insufficiency
topic Adrenoleukodystrophy
Peroxisomal disorders
Demyelinating diseases
Bone marrow transplantation
Aphasia
Adrenal insufficiency
description ABSTRACT Objective: To describe patients with different phenotypes of X-linked adrenoleukodystrophy: pre-symptomatic, cerebral demyelinating inflammatory adrenoleukodystrophy, adrenomyeloneuropathy and adrenal insufficiency only. Methods: Specific data related to epidemiology, phenotype, diagnosis and treatment of 24 patients with X-linked adrenoleukodystrophy were collected. A qualitative cross-sectional and descriptive-exploratory analysis was performed using medical records from a reference center in Neuropediatrics in Curitiba, Brazil, as well as an electronic questionnaire. Results: The majority (79%) of patients had cerebral demyelinating inflammatory adrenoleukodystrophy, presenting aphasia, hyperactivity and vision disorders as the main initial symptoms. These symptoms appeared, on average, between six and seven years of age. There was a mean delay of 11 months between the onset of symptoms/signs and the diagnosis. Patients sought diagnosis mainly with neuropediatricians, and the main requested tests were dosage of very long chain fatty acids and brain magnetic resonance. Conclusions: All phenotypes of X-linked adrenoleukodystrophy, except for myelopathy in women, were presented in the studied population, which mainly consisted of children and adolescents. Prevalent signs and symptoms registered in the literature were observed. Most of the patients with cerebral demyelinating inflammatory adrenoleukodystrophy were not diagnosed in time for hematopoietic stem cell transplantation.
publishDate 2019
dc.date.none.fl_str_mv 2019-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822019000400465
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822019000400465
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1984-0462/;2019;37;4;00015
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade de Pediatria de São Paulo
publisher.none.fl_str_mv Sociedade de Pediatria de São Paulo
dc.source.none.fl_str_mv Revista Paulista de Pediatria v.37 n.4 2019
reponame:Revista Paulista de Pediatria (Ed. Português. Online)
instname:Sociedade de Pediatria de São Paulo (SPSP)
instacron:SPSP
instname_str Sociedade de Pediatria de São Paulo (SPSP)
instacron_str SPSP
institution SPSP
reponame_str Revista Paulista de Pediatria (Ed. Português. Online)
collection Revista Paulista de Pediatria (Ed. Português. Online)
repository.name.fl_str_mv Revista Paulista de Pediatria (Ed. Português. Online) - Sociedade de Pediatria de São Paulo (SPSP)
repository.mail.fl_str_mv pediatria@spsp.org.br||rpp@spsp.org.br
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