X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIES
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , |
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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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 |
status_str |
publishedVersion |
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 |
_version_ |
1750318251534974976 |