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Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy

Limb-girdle muscular dystrophies (LGMDs) is a heterogeneous group of muscular dystrophies that mostly affect the pelvic and shoulder girdle muscle groups. We report here a case of neuromuscular disease associated with Dupuytren's contracture, which has never been described before as cosegregati...

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Autores principales: Lace, Baiba, Inashkina, Inna, Micule, Ieva, Vasiljeva, Inta, Naudina, Maruta Solvita, Strautmanis, Jurgis, Stavusis, Janis, Jankevics, Eriks
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3760302/
https://www.ncbi.nlm.nih.gov/pubmed/24024053
http://dx.doi.org/10.1155/2013/254950
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author Lace, Baiba
Inashkina, Inna
Micule, Ieva
Vasiljeva, Inta
Naudina, Maruta Solvita
Strautmanis, Jurgis
Stavusis, Janis
Jankevics, Eriks
author_facet Lace, Baiba
Inashkina, Inna
Micule, Ieva
Vasiljeva, Inta
Naudina, Maruta Solvita
Strautmanis, Jurgis
Stavusis, Janis
Jankevics, Eriks
author_sort Lace, Baiba
collection PubMed
description Limb-girdle muscular dystrophies (LGMDs) is a heterogeneous group of muscular dystrophies that mostly affect the pelvic and shoulder girdle muscle groups. We report here a case of neuromuscular disease associated with Dupuytren's contracture, which has never been described before as cosegregating with an autosomal dominant type of inheritance. Dupuytren's contracture is a common disease, especially in Northern Europe. Comorbid conditions associated with Dupuytren's contracture are repetitive trauma to the hands, diabetes, and seizures, but it has never before been associated with neuromuscular disease. We hypothesize that patients may harbor mutations in genes with functions related to neuromuscular disease and Dupuytren's contracture development.
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spelling pubmed-37603022013-09-10 Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy Lace, Baiba Inashkina, Inna Micule, Ieva Vasiljeva, Inta Naudina, Maruta Solvita Strautmanis, Jurgis Stavusis, Janis Jankevics, Eriks Case Rep Neurol Med Case Report Limb-girdle muscular dystrophies (LGMDs) is a heterogeneous group of muscular dystrophies that mostly affect the pelvic and shoulder girdle muscle groups. We report here a case of neuromuscular disease associated with Dupuytren's contracture, which has never been described before as cosegregating with an autosomal dominant type of inheritance. Dupuytren's contracture is a common disease, especially in Northern Europe. Comorbid conditions associated with Dupuytren's contracture are repetitive trauma to the hands, diabetes, and seizures, but it has never before been associated with neuromuscular disease. We hypothesize that patients may harbor mutations in genes with functions related to neuromuscular disease and Dupuytren's contracture development. Hindawi Publishing Corporation 2013 2013-08-19 /pmc/articles/PMC3760302/ /pubmed/24024053 http://dx.doi.org/10.1155/2013/254950 Text en Copyright © 2013 Baiba Lace et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Lace, Baiba
Inashkina, Inna
Micule, Ieva
Vasiljeva, Inta
Naudina, Maruta Solvita
Strautmanis, Jurgis
Stavusis, Janis
Jankevics, Eriks
Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy
title Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy
title_full Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy
title_fullStr Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy
title_full_unstemmed Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy
title_short Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy
title_sort dupuytren's contracture cosegregation with limb-girdle muscle dystrophy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3760302/
https://www.ncbi.nlm.nih.gov/pubmed/24024053
http://dx.doi.org/10.1155/2013/254950
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