[Masticatory muscle hypertrophy].
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Biomedical subjects
Publications and source records attributed to M Millefiorini.
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Starting from a case they observed and from similar cases of literature, the authors underline the variability of clinical aspects of MDCF which in this case was associated with absence of both motorial acquisitions and skeletal alterations. They underline how their case is characterized by the presence and consistence of musculotendinous retractions and by muscular weakness.
On the ground of preceding researches carried out about myodystrophias, the authors studied the melituric symptomatology in both a group of myasthenic patients and a group of control. The chromatographic analysis and the dosage of some urinary carbohydrates, showed that there are not statistically significant differences between the group of myasthenic patients and that of controls.
Authors refer to a clinical case in which they observed the association of bilateral cervical ribs with aneurism of subclavian artery. They underline the high frequencey of occasional observations of anomalies of the thoracic outlet, and consider the possible pathogenetic mechanisms of the thoracic outlet syndrome and associated vascular damages.
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It is described a case of compression of the deep branch of radial nerve caused by a lipoma, in which the use of C.T. was very important from a diagnostic point of view. It is described the use of C.T. in the evaluation of musculoskeletal neoplasms.
Polycythemic syndromes, particularly (Polycythemia vera), often causes neurological symptoms, that sometimes are the first in the clinic. The authors analyze the various neurological symptoms that more frequently occur and their probable pathogenesis. The clinical case taken into consideration by the authors showed the same symptoms of the endocranial hypertension.
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