Written at February 16, 2009 on Español, translated to English and with a size of 2,881 bytes.
1.-Q is 1 neuropathy? D chronic disease etiology routinely characterized x symptoms varied sensory, motor and autonomic q appear as systemic illnesses q d complicqaciones include metabolic diseases, toxic, infectious, nutritional, neoplastic and immunologic tests. 2.-Q is axonal degeneration? Before the attacks the nerve may reaccionarpor axonal degeneration where the cylinder capacity x inetrrupcion d affects its continuity with the cell body may not have the trophism + remote segments. when the axon is affected myelin bands d degenerate secondarily. 3.-Q is thedemyelination. 1 second way is the reaction of nerve demyelination, here the myelin sheath degenerates of generating primary form slowing and nerve conduction block d and remyelination initiated function usually recovers quickly and completely. 4.-As classify neuropathies x time d evolution? Acuteneuropathy: those with evolution from days to 4 weeks d inflammatory etiology. Subacute peripheralneuropathy: time of evolution of several weeks. (drugs, environmental toxins, nutritional, drug addiction) Acute peripheral neuropathy:time of evolution goes to mases years and constitute distinct disease sisntoma 1. (Metabolic, cancer, autoimmune diseases, hereditary neuropathies) 5.-neuropathies are classified as type x nerves areinvolved. Predominant motor neuropathy, predominantly sensory neuropathy, motor sensory neuropathy and autonomic neuropathy. (Mario: diesmielinizante washes neuropathy, chronic neuropathy diesmielinizante, aguads axonal neuropathy axonal neuropathy and chronic) 6.-As neuropathies are classified as d x DISTRIBUTION? Mononeuritis simple single nerve affectation, d 1 mononeuritis multiple: multiple nerve injury noncontiguous d polyneuritis: design 1 efectacion diffuse, distal and symmetric d nerves. 7.-X-rated d cause peripheralneuropathy: Peripheral neuropathy acquired physical injury, tumors, toxins, infections, autoimmune disorders, nutritional deficiencies, alcoholism, metabolic disorders, systemic disease. Hereditary peripheral neuropathy: the + common disorders are 1 gpo d q is the disease known as Charcot-Marie-Tooth. Features include extreme weakness, weight loss d inf limb muscles and feet, abnormal gait, loss d d tendon reflexes and limb numbness d inf. 8.-Describe such as clinical manifestations d neuropathies. Sensory signs common in peripheral neuropathies
Español, translated to 
English and with a size of 2,881 bytes.
