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Self-Mutilation in Neurodegeneration with Brain Iron Accumulation

Neurodegeneration with brain iron accumulation (NBIA) is the term applied to a heterogeneous group of disorders resulting in iron deposition in the basal ganglia. Well-known phenotypic features are progressive regression with extra pyramidal involvement and a variable course. A 10-year-old child bor...

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Autores principales: Chandra, Sadanandavalli Retnaswami, Raj, Pawan, Issac, Thomas Gregor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458944/
https://www.ncbi.nlm.nih.gov/pubmed/26120159
http://dx.doi.org/10.4103/0019-5154.156387
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author Chandra, Sadanandavalli Retnaswami
Raj, Pawan
Issac, Thomas Gregor
author_facet Chandra, Sadanandavalli Retnaswami
Raj, Pawan
Issac, Thomas Gregor
author_sort Chandra, Sadanandavalli Retnaswami
collection PubMed
description Neurodegeneration with brain iron accumulation (NBIA) is the term applied to a heterogeneous group of disorders resulting in iron deposition in the basal ganglia. Well-known phenotypic features are progressive regression with extra pyramidal involvement and a variable course. A 10-year-old child born to consanguineous parents presented with progressive generalized opisthotonic dystonia, retrocollis, oromandibular dyskinesias, apraxia for swallowing, optic atrophy and severe self-mutilation of lips. MR imaging showed brain iron accumulation. Other causes of self-mutilation were excluded. Early infantile onset, ophisthotonic dystonia with oromandibular dyskinesias and characteristic MR images are suggestive of NBIA. There is only one case reported in the literature of self-mutilation in this condition.
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spelling pubmed-44589442015-06-26 Self-Mutilation in Neurodegeneration with Brain Iron Accumulation Chandra, Sadanandavalli Retnaswami Raj, Pawan Issac, Thomas Gregor Indian J Dermatol Case Report Neurodegeneration with brain iron accumulation (NBIA) is the term applied to a heterogeneous group of disorders resulting in iron deposition in the basal ganglia. Well-known phenotypic features are progressive regression with extra pyramidal involvement and a variable course. A 10-year-old child born to consanguineous parents presented with progressive generalized opisthotonic dystonia, retrocollis, oromandibular dyskinesias, apraxia for swallowing, optic atrophy and severe self-mutilation of lips. MR imaging showed brain iron accumulation. Other causes of self-mutilation were excluded. Early infantile onset, ophisthotonic dystonia with oromandibular dyskinesias and characteristic MR images are suggestive of NBIA. There is only one case reported in the literature of self-mutilation in this condition. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4458944/ /pubmed/26120159 http://dx.doi.org/10.4103/0019-5154.156387 Text en Copyright: © Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Chandra, Sadanandavalli Retnaswami
Raj, Pawan
Issac, Thomas Gregor
Self-Mutilation in Neurodegeneration with Brain Iron Accumulation
title Self-Mutilation in Neurodegeneration with Brain Iron Accumulation
title_full Self-Mutilation in Neurodegeneration with Brain Iron Accumulation
title_fullStr Self-Mutilation in Neurodegeneration with Brain Iron Accumulation
title_full_unstemmed Self-Mutilation in Neurodegeneration with Brain Iron Accumulation
title_short Self-Mutilation in Neurodegeneration with Brain Iron Accumulation
title_sort self-mutilation in neurodegeneration with brain iron accumulation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458944/
https://www.ncbi.nlm.nih.gov/pubmed/26120159
http://dx.doi.org/10.4103/0019-5154.156387
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