| CLF | cardiolipin fluorescent [antibody]; ceroid lipofuscinosis; cholesterol-lecithin flocculation |
|---|---|
| NCL | neuronal ceroid-lipofuscinosis; nucleolin |
| CCL | Canine ceroid-lipofuscinosis |
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| CL | Ceroid-lipofuscinosis |
| INCL | Infantile neuronal ceroid lipofuscinosis |
| JNCL | Juvenile neuronal ceroid lipofuscinosis |
| LINCL | Late infantile neuronal ceroid lipofuscinosis |
| lipofuscinosis | Abnormal storage of any one of a group of fatty pigments. Ceroid lipofuscinosis, cerebral sphingolipidosis, late juvenile type. Neuronal ceroid lipofuscinosis, a group of diseases characterised by accumulation of abnormal pigments in tissue (previously classified as cerebral sphingolipidoses). Major subtypes include chronic juvenile form (Batten disease), slowly progressive behaviour and visual symptoms, autosomal recessive inheritance; acute, late infantile form (Bielschowsky disease); autosomal recessive inheritance; chronic adult form (Kufs disease), variable inheritance; acute infantile form (Santavuori-Haltia disease), fulminating motor and mental deterioration often associated with myoclonic seizures. Minor forms have also been described. (05 Mar 2000) |
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| 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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| lipofuscinosis |
(lipo
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|