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fat deficiency

См. также в других словарях:

  • fat-deficiency disease — a condition characterized by cessation of growth and skin lesions that result when essential fatty acids (linolenic and linoleic acid) are absent from the diet …   Medical dictionary

  • Deficiency, hex-A — Deficiency of the enzyme hexosaminidase A, the cause of Tay Sachs disease. Hex A deficiency results in failure to process a lipid (a fat) which accumulates and is deposited in the brain and other tissues, to their detriment. The lipid that is… …   Medical dictionary

  • Deficiency, hexosaminidase A — Deficiency of the enzyme hexosaminidase A, the cause of Tay Sachs disease. Hex A deficiency results in failure to process a lipid (a fat) which accumulates and is deposited in the brain and other tissues, to their detriment. The lipid that is… …   Medical dictionary

  • fat — fatless, adj. fatlike, adj. /fat/, adj., fatter, fattest, n., v., fatted, fatting. adj. 1. having too much flabby tissue; corpulent; obese: a fat person. 2. plump; well fed: a good, fat chicken. 3. consisting of or containing fat; greasy; oily:… …   Universalium

  • Deficiency, FAO — Also known as the Sjogren Larsson syndrome, this is a genetic (inherited) disease usually characterized by a triad of clinical findings consisting of ichthyosis (thickened fish like skin), spastic paraplegia (spasticity of the legs) and mental… …   Medical dictionary

  • Deficiency, fatty alcohol: NAD+ oxidoreductase — Also known as the Sjogren Larsson syndrome, this is a genetic (inherited) disease usually characterized by a triad of clinical findings consisting of ichthyosis (thickened fish like skin), spastic paraplegia (spasticity of the legs) and mental… …   Medical dictionary

  • Deficiency, fatty aldehyde dehydrogenase — Also known as the Sjogren Larsson syndrome, this is a genetic (inherited) disease usually characterized by a triad of clinical findings consisting of ichthyosis (thickened fish like skin), spastic paraplegia (spasticity of the legs) and mental… …   Medical dictionary

  • Deficiency, FALDH — Also known as the Sjogren Larsson syndrome, this is a genetic (inherited) disease usually characterized by a triad of clinical findings consisting of ichthyosis (thickened fish like skin), spastic paraplegia (spasticity of the legs) and mental… …   Medical dictionary

  • Deficiency, sphingomyelinase — Also called Niemann Pick disease, this is a disorder of the metabolism of a lipid (fat) called sphingomyelin that usually causes the progressive development of enlargement of the liver and spleen (hepatosplenomegaly), swollen glands… …   Medical dictionary

  • Hex-A deficiency — Deficiency of the enzyme hexosaminidase A, the cause of Tay Sachs disease. Hex A deficiency results in failure to process a lipid (a fat) which accumulates and is deposited in the brain and other tissues, to their detriment. The lipid that is… …   Medical dictionary

  • Growth hormone deficiency — Infobox Disease Name = PAGENAME Caption = Growth hormone DiseasesDB = 5447 ICD10 = ICD10|E|23|0|e|20 ICD9 = ICD9|253.3 ICDO = OMIM = MedlinePlus = 001176 eMedicineSubj = med eMedicineTopic = 930 MeshID = D004393 Growth Hormone Deficiency is the… …   Wikipedia

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