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Case of Small Vessel Disease Associated with COL4A1 Mutations following Trauma
With this case report, we would like to heighten the awareness of clinicians about COL4A1 as a single-gene disorder causing cerebral small vessel disease and describe a previously unreported pathogenic missense substitution in COL4A1 (p.Gly990Val) and a new clinical presentation. We identified a het...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4478326/ https://www.ncbi.nlm.nih.gov/pubmed/26120313 http://dx.doi.org/10.1159/000431309 |
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author | Plancher, Joao McONeil Hufnagel, Robert B. Vagal, Achala Peariso, Katrina Saal, Howard M. Broderick, Joseph P. |
author_facet | Plancher, Joao McONeil Hufnagel, Robert B. Vagal, Achala Peariso, Katrina Saal, Howard M. Broderick, Joseph P. |
author_sort | Plancher, Joao McONeil |
collection | PubMed |
description | With this case report, we would like to heighten the awareness of clinicians about COL4A1 as a single-gene disorder causing cerebral small vessel disease and describe a previously unreported pathogenic missense substitution in COL4A1 (p.Gly990Val) and a new clinical presentation. We identified a heterozygous putatively pathogenic mutation of COL4A1 in a 50-year-old female with a history of congenital cataracts and glaucoma who presented with multiple diffusion-positive infarcts and areas of contrast enhancement following mild head trauma. We believe that this presentation of multiple areas of acute brain and vascular injury in the setting of mild head trauma is a new manifestation of this genetic disorder. Imaging findings of multiple acute infarcts and regions of contrast enhancement with associated asymptomatic old deep microhemorrhages and leukomalacia in adults after head trauma should raise a high suspicion for a COL4A1 genetic disorder. Radiographic patterns of significant leukoaraiosis and deep microhemorrhages can also be seen in patients with long-standing vasculopathy associated with hypertension, which our patient lacked. Our findings demonstrate the utility of genetic screening for COL4A1 mutations in young patients who have small vessel vasculopathy on brain imaging but who do not have significant cardiovascular risk factors. |
format | Online Article Text |
id | pubmed-4478326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-44783262015-06-26 Case of Small Vessel Disease Associated with COL4A1 Mutations following Trauma Plancher, Joao McONeil Hufnagel, Robert B. Vagal, Achala Peariso, Katrina Saal, Howard M. Broderick, Joseph P. Case Rep Neurol Published online: June, 2015 With this case report, we would like to heighten the awareness of clinicians about COL4A1 as a single-gene disorder causing cerebral small vessel disease and describe a previously unreported pathogenic missense substitution in COL4A1 (p.Gly990Val) and a new clinical presentation. We identified a heterozygous putatively pathogenic mutation of COL4A1 in a 50-year-old female with a history of congenital cataracts and glaucoma who presented with multiple diffusion-positive infarcts and areas of contrast enhancement following mild head trauma. We believe that this presentation of multiple areas of acute brain and vascular injury in the setting of mild head trauma is a new manifestation of this genetic disorder. Imaging findings of multiple acute infarcts and regions of contrast enhancement with associated asymptomatic old deep microhemorrhages and leukomalacia in adults after head trauma should raise a high suspicion for a COL4A1 genetic disorder. Radiographic patterns of significant leukoaraiosis and deep microhemorrhages can also be seen in patients with long-standing vasculopathy associated with hypertension, which our patient lacked. Our findings demonstrate the utility of genetic screening for COL4A1 mutations in young patients who have small vessel vasculopathy on brain imaging but who do not have significant cardiovascular risk factors. S. Karger AG 2015-06-02 /pmc/articles/PMC4478326/ /pubmed/26120313 http://dx.doi.org/10.1159/000431309 Text en Copyright © 2015 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Distribution permitted for non-commercial purposes only. |
spellingShingle | Published online: June, 2015 Plancher, Joao McONeil Hufnagel, Robert B. Vagal, Achala Peariso, Katrina Saal, Howard M. Broderick, Joseph P. Case of Small Vessel Disease Associated with COL4A1 Mutations following Trauma |
title | Case of Small Vessel Disease Associated with COL4A1 Mutations following Trauma |
title_full | Case of Small Vessel Disease Associated with COL4A1 Mutations following Trauma |
title_fullStr | Case of Small Vessel Disease Associated with COL4A1 Mutations following Trauma |
title_full_unstemmed | Case of Small Vessel Disease Associated with COL4A1 Mutations following Trauma |
title_short | Case of Small Vessel Disease Associated with COL4A1 Mutations following Trauma |
title_sort | case of small vessel disease associated with col4a1 mutations following trauma |
topic | Published online: June, 2015 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4478326/ https://www.ncbi.nlm.nih.gov/pubmed/26120313 http://dx.doi.org/10.1159/000431309 |
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