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Neurodegeneration with Brain Iron Accumulation: Diagnosis and Management

Neurodegeneration with brain iron accumulation (NBIA) encompasses a group of inherited disorders that share the clinical features of an extrapyramidal movement disorder accompanied by varying degrees of intellectual disability and abnormal iron deposition in the basal ganglia. The genetic basis of t...

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Detalles Bibliográficos
Autor principal: Hogarth, Penelope
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Movement Disorder Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298713/
https://www.ncbi.nlm.nih.gov/pubmed/25614780
http://dx.doi.org/10.14802/jmd.14034
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author Hogarth, Penelope
author_facet Hogarth, Penelope
author_sort Hogarth, Penelope
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description Neurodegeneration with brain iron accumulation (NBIA) encompasses a group of inherited disorders that share the clinical features of an extrapyramidal movement disorder accompanied by varying degrees of intellectual disability and abnormal iron deposition in the basal ganglia. The genetic basis of ten forms of NBIA is now known. The clinical features of NBIA range from rapid global neurodevelopmental regression in infancy to mild parkinsonism with minimal cognitive impairment in adulthood, with wide variation seen between and within the specific NBIA sub-type. This review describes the clinical presentations, imaging findings, pathologic features, and treatment considerations for this heterogeneous group of disorders.
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spelling pubmed-42987132015-01-22 Neurodegeneration with Brain Iron Accumulation: Diagnosis and Management Hogarth, Penelope J Mov Disord Review Article Neurodegeneration with brain iron accumulation (NBIA) encompasses a group of inherited disorders that share the clinical features of an extrapyramidal movement disorder accompanied by varying degrees of intellectual disability and abnormal iron deposition in the basal ganglia. The genetic basis of ten forms of NBIA is now known. The clinical features of NBIA range from rapid global neurodevelopmental regression in infancy to mild parkinsonism with minimal cognitive impairment in adulthood, with wide variation seen between and within the specific NBIA sub-type. This review describes the clinical presentations, imaging findings, pathologic features, and treatment considerations for this heterogeneous group of disorders. The Korean Movement Disorder Society 2015-01 2015-01-13 /pmc/articles/PMC4298713/ /pubmed/25614780 http://dx.doi.org/10.14802/jmd.14034 Text en Copyright © 2015 The Korean Movement Disorder Society
spellingShingle Review Article
Hogarth, Penelope
Neurodegeneration with Brain Iron Accumulation: Diagnosis and Management
title Neurodegeneration with Brain Iron Accumulation: Diagnosis and Management
title_full Neurodegeneration with Brain Iron Accumulation: Diagnosis and Management
title_fullStr Neurodegeneration with Brain Iron Accumulation: Diagnosis and Management
title_full_unstemmed Neurodegeneration with Brain Iron Accumulation: Diagnosis and Management
title_short Neurodegeneration with Brain Iron Accumulation: Diagnosis and Management
title_sort neurodegeneration with brain iron accumulation: diagnosis and management
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298713/
https://www.ncbi.nlm.nih.gov/pubmed/25614780
http://dx.doi.org/10.14802/jmd.14034
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