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单词 oxalosis
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oxalosis
oxalosis n.
Brit. /ˌɒksəˈləʊsɪs/
,
U.S. /ˌɑksəˈloʊsəs/
[compare French oxalose (dated 1952 in Robert Dict. alphabétique et analogique (1986))] either of two inherited (autosomal recessive) metabolic disorders in which there is excessive oxalate excretion in the urine, with deposition of oxalate crystals in the kidneys and other organs and (esp. in the more severe form) renal failure in early life.
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the world > health and disease > ill health > a disease > disorders of internal organs > metabolic disorders > [noun] > other metabolic disorders
xanthomatosis1900
Tay-Sachs1907
ketosis1917
protein shock1917
hyperinsulinism1924
Niemann–Pick1928
tyrosinosis1932
von Gierke's disease1933
phenylketonuria1935
cystic fibrosis1938
mucoviscidosis1945
cystinosis1949
oxalosis1952
McArdle1957
orotic aciduria1959
PKU1961
sphingolipidosis1962
Reye's syndrome1965
Menkes1969
1952 L. Ying Chou & W. L. Donohue in Pediatrics 10 660 (title) Oxalosis. Possible ‘inborn error of metabolism’ with nephrolithiasis and nephrocalcinosis due to calcium oxalate as the predominating features.
1973 N. M. R. Buist et al. in J. Forfar & C. Arneil Textbk. Pediatrics xix. 1171/2 Treatment of oxalosis includes alkalinization of the urine, dietary restriction of calcium and a large fluid intake.
2002 Star (Sheffield) (Nexis) 12 Sept. Melanie became ill at the age of 16 with a rare condition called oxalosis. Her body was missing an enzyme and this caused crystals to grow in her kidneys—causing kidney failure.
extracted from oxalo-comb. form
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