| MELAS Syndrome | 1. Mitochondrial Encephalomyopathy 2. Lactic Acidosis 3. S... |
|---|---|
| RTA | Renal Tubular Acidosis |
| CMA | Canadian Medical Association; Certified Medical Assistant; chronic metabolic acidosis; cow's milk al... |
| DA | dark adaptation; dark agouti [rat]; daunomycin; degenerative arthritis; delayed action; Dental Assis... |
| MELAS | mitochondrial encephalomyopathy-lactic acidosis- and stroke-like symptoms [syndrome] |
| RTA | Renal Tubular Acidosis |
|---|---|
| LAT | lactic acidosis threshold |
| MELAS | myopathy, encephalopathy, lactic acidosis and stroke like episodes |
| hyperchloraemic acidosis | <nephrology> A rare sometimes familial disorder of the renal tubule characterised by the inability to excrete urine of normal acidity. This leads to a hyperchloraemic acidosis which is often associated with one or more secondary complications such as hypercalcinuria with nephrolithiasis and nephrocalcinosis, rickets, or osteomalacia and severe potassium depletion. (25 Jun 1999) |
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| starvation acidosis | Ketoacidosis resulting from lack of food intake, leading to fat catabolism to provide energy, releasing acidic ketone bodies. (05 Mar 2000) |
| diabetic acidosis | Decreased pH and bicarbonate concentration in the body fluids caused by accumulation of ketone bodies in diabetes mellitus. (05 Mar 2000) |
| osteopetrosis with renal tubular acidosis | <syndrome> An inherited deficiency of carbonic anhydrase II that results in osteopetrosis and metabolic acidosis. Synonym: osteopetrosis with renal tubular acidosis. (05 Mar 2000) |
| uncompensated acidosis | An acidosis in which the pH of body fluids is subnormal, because restoration of normal acid-base balance is not possible or has not yet been achieved. (05 Mar 2000) |
| lactic acidosis | <biochemistry, physiology> Acidosis caused by accumulation of lactic acid more rapidly than it can be metabolised. It may occur spontaneously or in association with diseases such as diabetes mellitus, leukaemia, or liver failure. (25 Jun 1999) |