| 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) |
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| 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) |
| ganglia aorticorena´lia |
[TA] aorticorenal ganglia: a more or less detached inferolateral extension of the celiac ganglion.
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| ganglia of autonomic plexuses |
ganglia plexuum autonomicorum.
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| ganglia of sympathetic trunk |
ganglia trunci sympathetici.
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| ganglia of visceral plexuses |
ganglia plexuum autonomicorum.
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| ganglial |
pertaining to a ganglion.
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