| gangliosidoses | <disease, neurology> Diseases, such as Tay Sachs, caused by inherited deficiency in enzymes necessary for the breakdown of gangliosides. Cause gross pathological changes in the nervous system, with devastating neurological symptoms. (18 Nov 1997) |
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| gangliosidosis | Any disease characterised, in part, by the abnormal accumulation within the nervous system of specific gangliosides, e.g., GM2 gangliosidosis, Tay-Sachs disease, caused by hexosaminidase A enzyme deficiency with accumulation of GM2 ganglioside Synonym: gangliosialidosis, ganglioside lipidosis. (05 Mar 2000) |
| gangliosidosis g(m1) | Form of gangliosidosis characterised by accumulation of g(m1) ganglioside and oligosaccharides, and caused by an absence or severe deficiency of beta-galactosidase a. The three phenotypes of g(m1) gangliosidosis are called infantile (generalised), juvenile, and adult (types 1, 2, and 3 respectively), referring to the age at which clinical manifestations appear. (12 Dec 1998) |
| ganglionectomy |
is a procedure in which the doctor removes a cyst from your hand, wrist, foot, or other part of your body.
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| ganglioglioneuroma |
Ganglion cells, glia cells, and nerve fibers in a nerve tumor.
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| ganglion neuron |
A neuron of the retina that receives impulses from bipolar neurons. Axons of ganglion neurons converge at the optic disk to form the optic nerve. SEE: retina for illus..
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| ganglionated neuroma |
Neuroma composed of true nerve cells.
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| ganglioplegia |
The failure of nervous stimuli to be transmitted by a ganglion. SEE: blockade, ganglionic.
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