期刊论文详细信息
BMC Musculoskeletal Disorders
Orthopaedic Disorders in Myotonic Dystrophy Type 1: descriptive clinical study of 21 patients
Albert Fujak1  Jürgen Forst1  Raimund Forst1  Lisa Schilling1 
[1] Department of Orthopaedic Surgery, Friedrich-Alexander-Universität Erlangen-Nürnberg, Rathsberger Str. 57, Erlangen D-91054, Germany
关键词: Pulmonary involvement;    Cardiac involvement;    Orthopaedic treatment;    Fractures;    Contractures;    Foot deformities;    Spinal deformities;    Orthopaedic disorders;    Curschmann-steinert disease;    Myotonic dystrophy type 1;   
Others  :  1129119
DOI  :  10.1186/1471-2474-14-338
 received in 2013-10-20, accepted in 2013-11-26,  发布年份 2013
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【 摘 要 】

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.

【 授权许可】

   
2013 Schilling et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Hebert LJ, Remec JF, et al.: The use of muscle strength assessed with handheld dynamometers as a non-invasive biological marker in myotonic dystrophy type 1 patients: a multicenter study. BMC Musculoskelet Disord 2010, 11:72. BioMed Central Full Text
  • [2]Canavese F, Sussman MD: Orthopaedic manifestations of congenital myotonic dystrophy during childhood and adolescence. J Pediatr Orthop 2009, 29:208-213.
  • [3]Bird TD: Myotonic Dystrophy Type 1. In GeneReviews™ [Internet]. Edited by Pagon RA, Adam MP, Bird TD, Dolan CR, Fong CT, Stephens K. Seattle (WA): University of Washington, Seattle; 1993–2013. 1999 Sep 17 [updated 2013 May 16]
  • [4]Wheeler TM, Lueck JD, et al.: Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy. J Clin Invest 2007, 117:3952-3957.
  • [5]Fayssoil A, Nardi O: Sudden death in Steinert’s disease. Int J Cardiol 2009, 136:27-28.
  • [6]Groh WJ, Groh MR, et al.: Electrocardiographic abnormalities and sudden death in myotonic dystrophy type 1. N Engl J Med 2008, 358:2688-2697.
  • [7]Cobo AM, Poza JJ, et al.: Frequency of myotonic dystrophy gene carriers in cataract patients. J Med Genet 1996, 33:221-223.
  • [8]Themistocleous GS, Sapkas GS, et al.: Scoliosis in Steinert syndrome: a case report. Spine J 2005, 5:212-216.
  • [9]Rutherford MA, Heckmatt JZ, et al.: Congenital myotonic dystrophy: respiratory function at birth determines survival. Arch Dis Child 1989, 64:191-195.
  • [10]Cup EH, Kinebanian A, et al.: Living with myotonic dystrophy; what can be learned from couples? A qualitative study. BMC Neurol 2011, 11:86. BioMed Central Full Text
  • [11]Asbach S, Gutleben KJ, et al.: Myotonic dystrophy initially presenting as tachycardiomyopathy successful catheter ablation of atrial flutter. Cardiol Res Pract 2010, 2010:383852. 4 pages
  • [12]Kaminsky P, Poussel M, et al.: Organ dysfunction and muscular disability in myotonic dystrophy type 1. Medicine 2011, 90:262-268.
  • [13]Reardon W, MacMillan JC, et al.: Cataract and myotonic dystrophy: the role of molecular diagnosis. Br J Ophthalmol 1993, 77:579-583.
  • [14]Dimeglio A: Growth in pediatric orthopaedics. J Pediatr Orthop 2001, 21:549-555.
  • [15]de Die-Smulders CE, Howeler CJ, et al.: Age and causes of death in adult-onset myotonic dystrophy. Brain 1998, 121:1557-1563.
  • [16]Daher YH, Lonstein JE, et al.: Spinal deformities in patients with muscular dystrophy other than Duchenne. A review of 11 patients having surgical treatment. Spine 1985, 10:614-617.
  • [17]Griffet J, Decrocq L, et al.: Lower extremity surgery in muscular dystrophy. Orthop Traumatol Surg Res 2011, 97:634-638.
  • [18]Mathieu J, Allard P, et al.: Anesthetic and surgical complications in 219 cases of myotonic dystrophy. Neurology 1997, 49:1646-1650.
  • [19]Sinclair JL, Reed PW: Risk factors for perioperative adverse events in children with myotonic dystrophy. Paediatr Anaesth 2009, 19:740-747.
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