Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0027121 (myositis)
 4,538 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

These guidelines propose performance criteria for the history and examination of patients with temporomandibular (TM) disorders. Pertinent diagnostic subcategories are identified, and the comprehensive history and review of systems are described. The examination procedures include documentation of temporomandibular and craniocervical range of motion, TM joint sounds, and the recording of muscle and joint tenderness. The TM disorders addressed include muscle problems such as myalgia, protective splinting or trismus, spasm, myositis, dyskinesia, muscle contracture, hypertrophy, and bruxism. Temporomandibular joint disorders addressed include disk-condyle incoordination, restricted condyle translation, open condyle dislocation, arthralgia, osteoarthritis, polyarthritis, and traumatic joint injury. Disorders of mandibular mobility such as ankylosis, adhesions, fibrosis, skeletal obstruction, and hypermobility are also described. Finally, disorders of maxillomandibular growth, including masticatory muscle hypertrophy, atrophy, neoplasia, maxillomandibular hypoplasia, condylar agenesis, maxillomandibular hyperplasia, and condyle hypertrophy are described.
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PMID:Guidelines for the examination and diagnosis of temporomandibular disorders. 260 95

A 16-year-old girl, one of dizygotic twins, presented in 1976 complaining of a 1-year history of a lack of coordination and an inability to run. The results of biochemical tests confirmed the diagnosis of classic abetalipoproteinemia. In addition to the recognized neurologic features of this disorder, she had a reduced evoked motor unit potential and markedly elevated serum levels of muscle enzymes, which suggested myositis. The serum vitamin E level was markedly decreased. Oral therapy with vitamin E, 800 mg daily, was begun, and in 1981 the dosage was increased to 3200 mg daily. Over the 7 years of follow-up she improved clinically, there was an increase in the evoked motor unit potential, the serum levels of some of the muscle enzymes decreased to normal, and the serum and tissue vitamin E levels increased significantly. It was concluded that treatment with high doses of vitamin E was responsible for the arrest of the usually progressive neuropathy and myopathy.
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PMID:Arrest of neuropathy and myopathy in abetalipoproteinemia with high-dose vitamin E therapy. 298 Nov 35