Axial myopathic syndrome
نویسندگان
چکیده
منابع مشابه
Freeman-Sheldon syndrome: a disorder of congenital myopathic origin?
Freeman-Sheldon syndrome was diagnosed in an unrelated adult man and woman, with severe abnormalities of the extremities but only slight anomalies of the face. Electromyography and muscle biopsy showed a myopathy which was classified as a congenital disproportion of fibre type and seemed to be the primary cause of the deformities. This allowed classification of the syndrome as a separate type o...
متن کاملTel Hashomer camptodactyly syndrome: report of a case with myopathic features.
A child with the Tel Hashomer camptodactyly syndrome is reported. Although muscle weakness and hypoplasia are reported features of this syndrome, further investigation of muscle function has not previously been carried out. We report a raised creatine kinase and an abnormal electromyogram and muscle biopsy in this syndrome. The histology of the muscle biopsy shows a wide range fibre diameter in...
متن کاملMyopathic changes associated with severe acute respiratory syndrome: a postmortem case series.
BACKGROUND The March 2003 outbreak of the severe acute respiratory syndrome (SARS) resulted in significant morbidity and mortality. Muscle weakness and elevated serum creatine kinase levels are commonly encountered in patients with SARS. However, the nature and cause of myopathy associated with a SARS infection are unknown because, to our knowledge, there has been no report of histological or p...
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The nervous system, unlike other body systems, is comprised of myriad subparts that typically have unique neuroanatomical and neurophysiological functions. Accordingly, localizing lesions within different areas of the nervous system can be quite a challenge. This task is made easier by utilizing the neurological syndrome approach. A "syndrome" is defined as a group of clinical signs that are us...
متن کاملExacerbation of symptoms due to diltiazem in a patient with Lambert-Eaton myasthenic myopathic syndrome.
A 65-year old man on treatment for ischaemic heart disease presented with a history of pain and weakness of all four limbs and dry mouth. He had clinical and neurophysiological features of Lambert-Eaton myasthenic syndrome. His symptoms improved after withdrawal of diltiazem, although neurophysiological changes remained even after 3 months.
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ژورنال
عنوان ژورنال: Annals of Physical and Rehabilitation Medicine
سال: 2011
ISSN: 1877-0657
DOI: 10.1016/j.rehab.2011.07.600