Polymyositis 7 year life expectancy
[DOC File]Muscleweakness can be either neurogenic or myogenic
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Prognosis. The life expectancy is markedly lowered; most patients die around age 50. Congenital Myotonic Dystrophy. This disease is due to a genetic defect involving a very large trinucleotide expansion (more than 2000 copies). It is usually passed on from mothers to their children, particularly when the mother already possesses a long expansion.
[DOC File]PART 17 - Mike South
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Life expectancy. Children with mild and moderate cerebral palsy have a normal life span. Those with severe motor impairment, particularly those who are wheelchair dependent and require tube feeding, have a reduced life expectancy. Chronic lung disease is the most common cause of morbidity and mortality in this group. Practical points
[DOCX File]PART 1 – APPLICANT DETAILS
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Severity of symptoms and life expectancy varies widely. CMT is characterised by progressive distal weakness and wasting, a high stepping gait, foot deformities, absent deep tendon reflexes and distal sensory loss, with symptoms usually beginning in early childhood or early adulthood, but can also be late onset (Menezes & North 2012).
[DOCX File]www.avtcp.org
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Life span. Average body weight. Body temperature. Heart rate. Respiratory rate. Sexual maturity . ... Polymyositis. Polyoma Virus . Porphyrinuria/pigmented urine . Pre-ovulatory egg binding. ... Average life expectancy for captive pet species. Grooming Needs. Which species may need grooming (nails/claws, feathers, beaks, etc) ...
[DOC File]Pathology - IHMC Public Cmaps (2)
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classic DM picture / 7, DRW53. Polymyositis. Onset usually > 50 yrs. Genetics: HLA-DR3, DQA1*0501 (whites and blacks), 0401 (blacks) Mechanism: CD8 T-cell mediated destruction. Muscle: inflammatory myopathy. Lungs: pulmonary inflammation / mostly CD8, some CD4. Heart: can get cardiomyopathy (even heart block) Diagnosis: clinical, EMG, biopsy
[DOC File]1)_PUBLIC HEALTH
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( 15-40% 5 year death rate depending on where Treatment is sought c. Polymyositis: • Generally occurs after 20 years of age & is due to T cells damaging the Muscle fibres directly. Unlike Dermatomyositis there is no Microangiopathy. ( There will be necrosis, phagocytosis, regeneration & fibrosis.
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