Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0003090 (arthrodesis)
 8,374 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

This paper reports three females and two males with a distinctive congenital syndrome characterized by severe congenital hypotonia, facial diplegia, jaw ankylosis, velo-pharyngeal incoordination, pyramidal tract signs, and ocular motor apraxia. Patients were followed up at ages ranging from 20 months to 16 years. All cases of this syndrome are sporadic, without dysmorphological features, chromosomal, or MRI brain abnormalities. Electrophysiological studies indicate the brainstem as the site of the neurological dysfunction. Post-mortem CNS study of one of the patients demonstrated neuronal depletion of the IV, VII, VIII, and IX cranial nerve nuclei and intact morphology of the cerebral hemispheres. A vascular accident, early in foetal life, is the most likely cause of the clinical picture. The extent of brainstem involvement and its related clinical findings distinguishes these patients from those with Moebius, Pierre Robin, or Cogan syndromes. Outcome is better than what could be anticipated during the first few months of life given the severity of symptoms. Intelligence or developmental quotients are within the normal range for their age. Facial hypomimia, feeding, and speech articulatory performance difficulties are the main disabilities observed in these patients at follow-up.
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PMID:Brainstem dysgenesis: report of five patients with congenital hypotonia, multiple cranial nerve involvement, and ocular motor apraxia. 1282 4