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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Movement Disorder Society
2015
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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 |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-4298713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Korean Movement Disorder Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT hogarthpenelope neurodegenerationwithbrainironaccumulationdiagnosisandmanagement |