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torticollis/atrophy
Veza se sprema u međuspremnik
Stranica 1 iz 107 rezultatima
Painful torticollis with tongue atrophy--a different neck-tongue syndrome.
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Two children were referred with neck pain, torticollis, dysarthria, and atrophy of the tongue. The erythrocyte sedimentation rate was markedly elevated in both cases. Radiologic appearances were similar. In both cases the cervical spine was stable. Computerised tomography showed soft-tissue swelling
Severe dysphagia after botulinum toxin injection for cervical dystonia in multiple system atrophy.
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A 71-year-old woman was treated by botulinum toxin (BTX) type A injections for cervical dystonia related to a multiple system atrophy (MSA). A few days later and persisting for the next 4 months, she developed a severe dysphagia, requiring nasogastric feeding. This implicates cautious use of BTX in
Fibrosis, adipogenesis, and muscle atrophy in congenital muscular torticollis.
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In the traditional view, muscle atrophy and interstitial fibrosis were regarded as the basic pathological features of congenital muscular torticollis (CMT). But in the ultrastructure study, the mesenchyme-like cells, myoblasts, myofibroblasts, and fibroblasts were found in the proliferation of
Cervical dystonia in dentatorubral-pallidoluysian atrophy.
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Hereditary dentatorubral-pallidoluysian atrophy (DRPLA) is a rare autosomal-dominant neurodegenerative disease characterized by variable clinical phenotypes. Its characteristic clinical manifestations include ataxia, choreoathetotic movements, seizures, myoclonus and dementia, but cervical dystonia
Muscle fiber atrophy in leg muscles after botulinum toxin type A treatment of cervical dystonia.
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Previous electrophysiologic studies on the effects of local injections of botulinum toxin type A (BTX-A) have indicated impaired neuromuscular transmission in distant muscles. To further study possible distant effects of repeated BTX-A injections, we obtained percutaneous muscle biopsies of the
[Oculo-facio-cervical dystonia syndrome revealed by plurisystematized degeneration of the central nervous system with pallidoreticular pigmentary condition].
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[Postural dystonia and spastic torticollis associated with an increase of cupriuria. Relations with hepato-lenticular degeneration].
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A Novel Missense OPA1 Mutation in a Patient with Dominant Optic Atrophy and Cervical Dystonia.
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Ultrastructure of the sternocleidomastoid muscle in muscular torticollis.
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The sternocleidomastoid muscles from five children with muscular torticollis--examined by transmission electron microscopy, exhibited a marked increase in interstitial collagen deposition, and scattered areas of amorphous ground substance with electron dense deposits. No vascular abnormalities were
Pathological features of idiopathic torticollis in the duck--a model for human disease.
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Light and electron microscopical observation of the neck muscles of ducks with torticollis are reported. Degeneration, inflammatory reaction, fatty infiltration and some regeneration were seen. The pathological features resemble those of human torticollis. This animal model provides an opportunity
Molecular mechanisms of treadmill therapy on neuromuscular atrophy induced via botulinum toxin A.
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Botulinum toxin A (BoNT-A) is a bacterial zinc-dependent endopeptidase that acts specifically on neuromuscular junctions. BoNT-A blocks the release of acetylcholine, thereby decreasing the ability of a spastic muscle to generate forceful contraction, which results in a temporal local weakness and
Acquired torticollis in eleven horses.
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Case records of 11 horses with acquired torticollis during a 15-year period were reviewed. The cause was established in seven of eight cases and included cervical intervertebral disk protrusion, skull fracture, neurogenic atrophy, and dystrophic myodegeneration. The latter condition was considered
Parry-Romberg syndrome presenting with recurrent exotropia and torticollis.
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Parry-Romberg syndrome, or progressive facial hemiatrophy, is a unilateral, slowly progressive atrophy that affects skin, subcutaneous tissues, muscles, and bones. The authors describe an 8-year-old girl with Parry-Romberg syndrome, amblyopia, recurrent exotropia, and torticollis, and stress that
Spondylotic myelopathy in patients with cervical dystonia.
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The treatment and outcome of cervical dystonia (CD) with myelopathy (CDM) varies among studies. We retrospectively reviewed the clinical features, neuroimages, methods of treatment, and modified Rankin scale (mRS) score of patients with CDM in our hospital. There were seven male and three female
[Aetiopathogenesis of scoliosis, hip dysplasia and torticollis in infancy (author's transl)].
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The special risk of the newborn to acquire, skeletal deformities is based on the increased plasticity, intensity of growth and extrapyramidal activity of reflexes which influence each other. These 3 factors may lead to structural growth- and weight bearing deformities in the presence of shrinking
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