Renal artery fibromuscular dysplasia in Pompe disease: A case report

Vascular involvement in Late Onset Pompe Disease, glycogen storage disease type II characterized by limb-girdle muscle and diaphragmatic weakness, is well documented. Abnormalities of posterior cerebral circulation have mostly been reported, whereas there are also cases of associated extracerebral a...

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Autores principales: Pappa, Evangelia, Papadopoulos, Constantinos, Grimbert, Philippe, Laforêt, Pascal, Bassez, Guillaume
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078050/
https://www.ncbi.nlm.nih.gov/pubmed/30090700
http://dx.doi.org/10.1016/j.ymgmr.2018.07.002
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author Pappa, Evangelia
Papadopoulos, Constantinos
Grimbert, Philippe
Laforêt, Pascal
Bassez, Guillaume
author_facet Pappa, Evangelia
Papadopoulos, Constantinos
Grimbert, Philippe
Laforêt, Pascal
Bassez, Guillaume
author_sort Pappa, Evangelia
collection PubMed
description Vascular involvement in Late Onset Pompe Disease, glycogen storage disease type II characterized by limb-girdle muscle and diaphragmatic weakness, is well documented. Abnormalities of posterior cerebral circulation have mostly been reported, whereas there are also cases of associated extracerebral arteriopathy. We report the case of a 42-year-old man diagnosed with LOPD a year after renal infarct due to renal artery fibromuscular dysplasia. We propose that the association of LOPD and arteriopathy should always be considered in clinical practice.
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spelling pubmed-60780502018-08-08 Renal artery fibromuscular dysplasia in Pompe disease: A case report Pappa, Evangelia Papadopoulos, Constantinos Grimbert, Philippe Laforêt, Pascal Bassez, Guillaume Mol Genet Metab Rep Case Report Vascular involvement in Late Onset Pompe Disease, glycogen storage disease type II characterized by limb-girdle muscle and diaphragmatic weakness, is well documented. Abnormalities of posterior cerebral circulation have mostly been reported, whereas there are also cases of associated extracerebral arteriopathy. We report the case of a 42-year-old man diagnosed with LOPD a year after renal infarct due to renal artery fibromuscular dysplasia. We propose that the association of LOPD and arteriopathy should always be considered in clinical practice. Elsevier 2018-07-26 /pmc/articles/PMC6078050/ /pubmed/30090700 http://dx.doi.org/10.1016/j.ymgmr.2018.07.002 Text en © 2018 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Pappa, Evangelia
Papadopoulos, Constantinos
Grimbert, Philippe
Laforêt, Pascal
Bassez, Guillaume
Renal artery fibromuscular dysplasia in Pompe disease: A case report
title Renal artery fibromuscular dysplasia in Pompe disease: A case report
title_full Renal artery fibromuscular dysplasia in Pompe disease: A case report
title_fullStr Renal artery fibromuscular dysplasia in Pompe disease: A case report
title_full_unstemmed Renal artery fibromuscular dysplasia in Pompe disease: A case report
title_short Renal artery fibromuscular dysplasia in Pompe disease: A case report
title_sort renal artery fibromuscular dysplasia in pompe disease: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078050/
https://www.ncbi.nlm.nih.gov/pubmed/30090700
http://dx.doi.org/10.1016/j.ymgmr.2018.07.002
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AT laforetpascal renalarteryfibromusculardysplasiainpompediseaseacasereport
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