Literature DB >> 8503797

Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients.

B Udd1, J Partanen, P Halonen, B Falck, L Hakamies, H Heikkilä, S Ingo, H Kalimo, H Kääriäinen, V Laulumaa.   

Abstract

OBJECTIVE: To clarify the classification of two previously reported groups of patients with anterior tibial distal dystrophy, to find additional patients with the disease, and to describe the clinical features of this disease.
DESIGN: National survey of the records of patients with neuromuscular diseases in Finland. Findings of selected patients were compared with those of previously reported cases. PATIENTS: Thirty-six previously described patients and 30 additional patients from the current survey, with 41 symptomatic patients and 25 subjectively asymptomatic affected relatives.
RESULTS: There were 66 patients with late adult-onset tibial muscular dystrophy. Symptoms appear after the age of 35 years with reduced ankle dorsiflexion, and progress is slow without marked disability. Facial muscles, upper extremities, and proximal muscles are usually spared. Muscle biopsy results reveal nonspecific dystrophic changes in clinically affected muscles, and frequently severe adipose replacement in the anterior tibial muscles occurs. Asymptomatic muscles have mild myopathic changes only. Vacuolar degeneration is detected in a minority of patients. Electromyography shows profound myopathic changes in the anterior tibial muscle, but extensor brevis muscles are well preserved. Computed tomography or magnetic resonance imaging of muscles discloses marked involvement of tibial extensor muscles and focal patches of fatty degeneration in various asymptomatic muscles. Pedigree data suggest autosomal dominant inheritance.
CONCLUSIONS: Tibial muscular dystrophy might represent a new form of distal myopathy and it is rather common, at least in Finland.

Entities:  

Mesh:

Year:  1993        PMID: 8503797     DOI: 10.1001/archneur.1993.00540060044015

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  27 in total

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5.  Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q.

Authors:  P Nicolao; F Xiang; L G Gunnarsson; B Giometto; L Edström; M Anvret; Z Zhang
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6.  A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population.

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7.  Autosomal recessive distal muscular dystrophy.

Authors:  C Scoppetta; B Mercuri; R Di Lello; V S Tolli; G F Mennuni; M L Vaccario
Journal:  Ital J Neurol Sci       Date:  1997-10

8.  Assignment of the tibial muscular dystrophy locus to chromosome 2q31.

Authors:  H Haravuori; P Mäkelä-Bengs; B Udd; J Partanen; L Pulkkinen; H Somer; L Peltonen
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9.  Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin.

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Review 10.  Distal myopathies.

Authors:  Mazen M Dimachkie; Richard J Barohn
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