| CLF | cardiolipin fluorescent [antibody]; ceroid lipofuscinosis; cholesterol-lecithin flocculation |
|---|---|
| NCL | neuronal ceroid-lipofuscinosis; nucleolin |
| CCL | Canine ceroid-lipofuscinosis |
|---|---|
| CL | Ceroid-lipofuscinosis |
| INCL | Infantile neuronal ceroid lipofuscinosis |
| JNCL | Juvenile neuronal ceroid lipofuscinosis |
| LINCL | Late infantile neuronal ceroid lipofuscinosis |
| ceroid | A naturally occurring lipid pigment with histochemical characteristics similar to lipofuscin. It accumulates in various tissues in certain experimental and pathological conditions. (12 Dec 1998) |
|---|---|
| ceroidosis | <radiology> Brown bowel syndrome, diffuse accumulation of brown lipofuscin pigment in muscularis propria of GI tract, secondary to chronic malabsorption and depletion of vitamin E, dilatation and hypomotility of entire GI tract can simulate obstruction (12 Dec 1998) |
| neuronal ceroid-lipofuscinosis | A heritable lipidosis with cytoplasmic inclusions staining for ceroid and lipofuscin. Clinically the patient has progressive dementia, retinal degeneration, seizures, and myoclonic jerks. It was formerly thought to be related to tay-sachs disease but the biochemical defect is as yet undetermined. Named according to age of onset: jansky-bielschowsky disease, 2-4 years; batten-spielmeyer-vogt disease, 5-11 years; and kufs disease, adult. (12 Dec 1998) |
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Synonyms :
| ceroid-lipofuscinosis |
neuronal ceroid-lipofuscinosis, a term for several genetic lipidoses of diverse biochemical and clinical characteristics, all characterized by progressive neurodegeneration, loss of vision, and a fatal course; the infantile type is Haltia-Santavuori disease; the late infantile type is Jansky-Bielschowsky disease; the juvenile type is Vogt-Spielmeyer disease; and the adult type is Kufs' disease. Formerly called also amaurotic familial idiocy.
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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| ceroid |
wax-like material found as crystals in disease states
Ãâó: www.southalabama.edu/alliedhealth/cls/Ravine/gloss...
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| ceroid-l. |
a term for several genetic lipidoses of diverse biochemical and clinical characteristics, all characterized by progressive neurodegeneration, loss of vision, and a fatal course; the infantile type is Haltia-Santavuori disease; the late infantile type is Jansky-Bielschowsky disease; the juvenile type is Vogt-Spielmeyer disease; and the adult type is Kufs' disease. Formerly called also amaurotic familial idiocy.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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