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L/S ratio Lecithin/Sphingomyelin
  > 2À̳ª IRDS°¡ ¿À´Â °æ¿ì
  1. DM Mother
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L/S lactase/sucrase [ratio]; lecithin/ sphingomyelin [ratio]; lipid/saccharide [ratio]; longitudinal sec...
LSR lanthanide shift reagent; lecithin/ sphingomyelin ratio; left superior rectus [muscle]; liver/spleen...
SM Master of Science; sadomasochism; self-monitoring; silicon microphysiometer; simple mastectomy; skim...
SPH secondary pulmonary hemosiderosis; severely and profoundly handicapped; spherocyte; spherocytosis; s...
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L/S Lecithin-Sphingomyelin
L/S lecithin/sphingomyelin ration
L/S ratio Lecithin/sphingomyelin ratio
SM Sphingomyelin
SP Sphingomyelin
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galactosylceramide lipoidosis <radiology> Dysmyelinating disease, autosomal recessive, usually presents by 1 yr, specific enzyme deficiency identified, rapid spontaneous nystagmus, poikilothermia
Synonym: Krabbe leukodystrophy
(12 Dec 1998)
lipoidosis A disturbance of lipid metabolism with abnormal deposit of lipids in the cells.
(12 Dec 1998)
lipoidosis corneae An opaque, grayish ring at the periphery of the cornea just within the sclerocorneal junction, of frequent occurrence in the aged; it results from a deposit of fatty granules in, or hyaline degeneration of, the lamellae and cells of the cornea.
Synonym: anterior embryotoxon, arcus adiposus, arcus juvenilis, arcus lipoides, arcus senilis, gerontoxon, linea corneae senilis, lipoidosis corneae.
(05 Mar 2000)
lipoidosis cutis et mucosae <disease> A familial disease occurring in the course of latent diabetes, marked by yellowish nodules due to deposits of a protein-lipid complex on the oral tongue and sublingual and faucial areas, translucent keratotic papillomatous eyelid lesions, keratotic lesions on the extremities, and hoarseness.
It is due to a disturbance of lipid metabolism with autosomal recessive inheritance and is frequently associated with intracranial calcifications.
inheritance: autosomal recessive.
Synonym: hyalinasis cutis et mucosae, lipoidosis cutis et mucosae, Urbach-Wiethe disease.
(05 Mar 2000)
sphingomyelin <biochemistry> A sphingolipid in which the head group is phosphoryl choline. A close analogue of phosphatidylcholine. In many cells the concentration of sphingomyelin and phosphatidylcholine in the plasma membrane seems to bear a reciprocal relationship.
(18 Nov 1997)
sphingomyelin deacylase <enzyme> Forms sphingosylphosphocholine
Registry number: EC 3.5.1.-
Synonym: sm-deacylase
(26 Jun 1999)
sphingomyelin lipidosis <disease> A family of severe lysosomal storage diseases resulting in an accumulation of sphingomyelin and other phospholipids in the reticuloendothelial system.
The best studied forms are due to deficiency of sphingomyelinase and it is more common in Ashkenazi Jews than other groups.
Clinical signs include foam cells in the blood and marrow, hepatosplenomegaly and neurologic degeneration. Diagnosis is confirmed by enzyme assay on leukocytes or fibroblasts and specific mutations in the gene are now recognised.
(29 Dec 1997)
sphingomyelin phosphodiesterase <enzyme> An enzyme that catalyses the hydrolysis of sphingomyelin to ceramide (n-acylsphingosine) plus choline phosphate. A defect in this enzyme leads to niemann-pick disease.
Chemical name: Sphingomyelin cholinephosphohydrolase
Registry number: EC 3.1.4.12
(12 Dec 1998)
lecithin/sphingomyelin ratio A ratio used to determine foetal pulmonary maturity, found by testing the amniotic fluid; when the lungs are mature, lecithin exceeds sphingomyelin by 2 to 1.
(05 Mar 2000)
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