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Dilated cardiomyopathy in humans can be caused by multiple factors including hereditary defects in the cytoskeletal protein dystrophin in Duchenne muscular dystrophy (DMD) patients). A heart that undergoes dilated cardiomyopathy shows unique enlargement of ventricles, and thinning of the ventricular wall that may lead to heart failure.
Leigh syndrome (also called Leigh disease and subacute necrotizing encephalomyelopathy) is an inherited neurometabolic disorder that affects the central nervous system.It is named after Archibald Denis Leigh, a British neuropsychiatrist who first described the condition in 1951. [2]
It can be caused by a bacterial infection, such as bacterial meningitis, [17] or may be a complication of a current infectious disease such as syphilis (secondary encephalitis). [ 18 ] Other bacterial pathogens, like Mycoplasma and those causing rickettsial disease , cause inflammation of the meninges and consequently encephalitis.
N. fowleri can be grown in several kinds of liquid axenic media or on non-nutrient agar plates coated with bacteria. Escherichia coli can be used to overlay the non-nutrient agar plate and a drop of cerebrospinal fluid sediment is added to it. Plates are then incubated at 37 °C and checked daily for clearing of the agar in thin tracks, which ...
Noncompaction cardiomyopathy (NCC) is a rare congenital disease of heart muscle that affects both children and adults. [1] It results from abnormal prenatal development of heart muscle. [2] [3] During development, the majority of the heart muscle is a sponge-like meshwork of interwoven myocardial fibers.
Wernicke encephalopathy (WE), also Wernicke's encephalopathy, [1] or wet brain is the presence of neurological symptoms caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves, in particular thiamine (vitamin B 1). [2]
Arrhythmias not due to structural heart disease account for 5 to 10% of sudden cardiac arrests. [ 42 ] [ 43 ] [ 44 ] These are frequently caused by genetic disorders . [ 30 ] The genetic mutations often affect specialized proteins known as ion channels that conduct electrically charged particles across the cell membrane , and this group of ...
Encephalopathy is a difficult term because it can be used to denote either a disease or finding (i.e., an observable sign in a person). [citation needed] When referring to a finding, encephalopathy refers to permanent (or degenerative) [11] brain injury, or a reversible one. It can be due to direct injury to the brain, or illness remote from ...