Aug 22, 2003 23:34
21 yrs ago
angļu term
Methaemoglobinaemia
angļu - latviešu
Medicīna
Slimiiba tabulaa starp cianozi, hemoliizi, aneemiju utt. Bez konteksta.
Proposed translations
(latviešu)
5 | methemoglobinēmija |
Kristine Sprula (Lielause)
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3 | Metamoglobinēmija |
Uldis Liepkalns
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Proposed translations
8 dienas
Selected
methemoglobinēmija
Dr.med. Georgi Arnaudov
TERMINOLOGIA MEDICA POLYGLOTTA
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Note added at 2003-08-31 09:05:16 (GMT)
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p.s. vārdnīca latīņu-krievu-angļu-franču-vācu valodā
TERMINOLOGIA MEDICA POLYGLOTTA
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Note added at 2003-08-31 09:05:16 (GMT)
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p.s. vārdnīca latīņu-krievu-angļu-franču-vācu valodā
4 KudoZ points awarded for this answer.
Comment: "Wow :))))
Un kur Tu agraak biji, piemeeram, vakar ?????"
10 h
Metamoglobinēmija
IMHO- pēc manas pieredzes visi šitie tā pat arī latviski saucas...
http://cancerweb.ncl.ac.uk/cgi-bin/omd?query=Methaemoglobina...
methaemoglobinaemia
<haematology> A clinical condition in which more than 1% of the haemoglobin in the blood has been oxidized to the ferric (Fe3+) state. The principle finding is cyanosis due to the oxidized haemoglobins inability to transport oxygen. Nitrites can cause this condition and it has been reported in commercial meat packers. Treatment may include ascorbic acid or methylene blue.
It may be drug-induced or be due to a defect in the enzyme NADH methaemoglobin reductase (an autosomal recessive trait) or to an abnormality in haemoglobin M (an autosomal dominant trait).
http://cancerweb.ncl.ac.uk/cgi-bin/omd?query=Methaemoglobina...
methaemoglobinaemia
<haematology> A clinical condition in which more than 1% of the haemoglobin in the blood has been oxidized to the ferric (Fe3+) state. The principle finding is cyanosis due to the oxidized haemoglobins inability to transport oxygen. Nitrites can cause this condition and it has been reported in commercial meat packers. Treatment may include ascorbic acid or methylene blue.
It may be drug-induced or be due to a defect in the enzyme NADH methaemoglobin reductase (an autosomal recessive trait) or to an abnormality in haemoglobin M (an autosomal dominant trait).
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