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Orthopaedic Disorders in Myotonic Dystrophy Type 1: descriptive clinical study of 21 patients

BACKGROUND: Myotonic Dystrophy Type 1 (DM1) is the most common form of hereditary myopathy presenting in adults. This autosomal-dominant systemic disorder is caused by a CTG repeat, demonstrating various symptoms. A mild, classic and congenital form can be distinguished. Often the quality of life is...

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Autores principales: Schilling, Lisa, Forst, Raimund, Forst, Jürgen, Fujak, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219587/
https://www.ncbi.nlm.nih.gov/pubmed/24289806
http://dx.doi.org/10.1186/1471-2474-14-338
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author Schilling, Lisa
Forst, Raimund
Forst, Jürgen
Fujak, Albert
author_facet Schilling, Lisa
Forst, Raimund
Forst, Jürgen
Fujak, Albert
author_sort Schilling, Lisa
collection PubMed
description BACKGROUND: Myotonic Dystrophy Type 1 (DM1) is the most common form of hereditary myopathy presenting in adults. This autosomal-dominant systemic disorder is caused by a CTG repeat, demonstrating various symptoms. A mild, classic and congenital form can be distinguished. Often the quality of life is reduced by orthopaedic problems, such as muscle weakness, contractures, foot or spinal deformities, which limit patients’ mobility. The aim of our study was to gather information about the orthopaedic impairments in patients with DM1 in order to improve the medical care of patients, affected by this rare disease. METHODS: A retrospective clinical study was carried out including 21 patients (11 male and 10 female), all diagnosed with DM1 by genetic testing. All patients were seen during our special consultations for neuromuscular diseases, during which patients were interviewed and examined. We also reviewed surgery reports of our hospitalized patients. RESULTS: We observed several orthopaedic impairments: spinal deformities (scoliosis, hyperkyphosis, rigid spine), contractures (of the upper extremities and the lower extremities), foot deformities (equinus deformity, club foot, pes cavus, pes planovalgus, pes cavovarus, claw toes) and fractures. Five patients were affected by pulmonary diseases (obstructive airway diseases, restrictive lung dysfunctions). Twelve patients were affected by cardiac disorders (congenital heart defects, valvular heart defects, conduction disturbances, pulmonary hypertension, cardiomyopathy). Our patients received conservative therapy (physiotherapy, logopaedic therapy, ergotherapy) and we prescribed orthopaedic technical devices (orthopaedic custom-made shoes, insoles, lower and upper leg orthoses, wheelchair, Rehab Buggy). We performed surgery for spinal and foot deformities: the scoliosis of one patient was stabilized and seven patients underwent surgery for correction of foot deformities. CONCLUSIONS: An orthopaedic involvement in DM1 patients should not be underestimated. The most common orthopaedic impairments are contractures, foot deformities and spinal deformities. Contractures are typically located distally in the lower extremities, but can also occur in the hip or shoulder joints. Foot deformities could be treated with orthopaedic custom-made shoes, orthoses or insoles. Surgery is indicated for severe foot deformities or contractures.
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spelling pubmed-42195872014-11-05 Orthopaedic Disorders in Myotonic Dystrophy Type 1: descriptive clinical study of 21 patients Schilling, Lisa Forst, Raimund Forst, Jürgen Fujak, Albert BMC Musculoskelet Disord Research Article BACKGROUND: Myotonic Dystrophy Type 1 (DM1) is the most common form of hereditary myopathy presenting in adults. This autosomal-dominant systemic disorder is caused by a CTG repeat, demonstrating various symptoms. A mild, classic and congenital form can be distinguished. Often the quality of life is reduced by orthopaedic problems, such as muscle weakness, contractures, foot or spinal deformities, which limit patients’ mobility. The aim of our study was to gather information about the orthopaedic impairments in patients with DM1 in order to improve the medical care of patients, affected by this rare disease. METHODS: A retrospective clinical study was carried out including 21 patients (11 male and 10 female), all diagnosed with DM1 by genetic testing. All patients were seen during our special consultations for neuromuscular diseases, during which patients were interviewed and examined. We also reviewed surgery reports of our hospitalized patients. RESULTS: We observed several orthopaedic impairments: spinal deformities (scoliosis, hyperkyphosis, rigid spine), contractures (of the upper extremities and the lower extremities), foot deformities (equinus deformity, club foot, pes cavus, pes planovalgus, pes cavovarus, claw toes) and fractures. Five patients were affected by pulmonary diseases (obstructive airway diseases, restrictive lung dysfunctions). Twelve patients were affected by cardiac disorders (congenital heart defects, valvular heart defects, conduction disturbances, pulmonary hypertension, cardiomyopathy). Our patients received conservative therapy (physiotherapy, logopaedic therapy, ergotherapy) and we prescribed orthopaedic technical devices (orthopaedic custom-made shoes, insoles, lower and upper leg orthoses, wheelchair, Rehab Buggy). We performed surgery for spinal and foot deformities: the scoliosis of one patient was stabilized and seven patients underwent surgery for correction of foot deformities. CONCLUSIONS: An orthopaedic involvement in DM1 patients should not be underestimated. The most common orthopaedic impairments are contractures, foot deformities and spinal deformities. Contractures are typically located distally in the lower extremities, but can also occur in the hip or shoulder joints. Foot deformities could be treated with orthopaedic custom-made shoes, orthoses or insoles. Surgery is indicated for severe foot deformities or contractures. BioMed Central 2013-12-01 /pmc/articles/PMC4219587/ /pubmed/24289806 http://dx.doi.org/10.1186/1471-2474-14-338 Text en Copyright © 2013 Schilling et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Schilling, Lisa
Forst, Raimund
Forst, Jürgen
Fujak, Albert
Orthopaedic Disorders in Myotonic Dystrophy Type 1: descriptive clinical study of 21 patients
title Orthopaedic Disorders in Myotonic Dystrophy Type 1: descriptive clinical study of 21 patients
title_full Orthopaedic Disorders in Myotonic Dystrophy Type 1: descriptive clinical study of 21 patients
title_fullStr Orthopaedic Disorders in Myotonic Dystrophy Type 1: descriptive clinical study of 21 patients
title_full_unstemmed Orthopaedic Disorders in Myotonic Dystrophy Type 1: descriptive clinical study of 21 patients
title_short Orthopaedic Disorders in Myotonic Dystrophy Type 1: descriptive clinical study of 21 patients
title_sort orthopaedic disorders in myotonic dystrophy type 1: descriptive clinical study of 21 patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219587/
https://www.ncbi.nlm.nih.gov/pubmed/24289806
http://dx.doi.org/10.1186/1471-2474-14-338
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