| ¿µ¹® | osteomalacia | ÇÑ±Û | °ñ¿¬ÈÁõ |
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| ¿µ¹® | malabsorption | ÇÑ±Û | Èí¼öÀå¾Ö |
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| OM | obtuse mental; occipitomental; occupational medicine; ocular movement; oculomotor; Osborne Mendel [r... |
|---|---|
| IDA | 1) Imino-Diacetic Acid 2) Iron Deficiency Anemia &nb... |
| GGM | glucose-galactose malabsorption |
| LM | lactic acid mineral [medium]; lactose malabsorption; laryngeal mask; laryngeal muscle; lateral malle... |
| AM | Academic Medicine [journal]; actomyosin; acute myelofibrosis; adult male; adult monocyte; aerospace ... |
| OM | Osteomalacia |
|---|---|
| DUE | DNA unwinding element |
| DUE | Drug usage evaluation |
| AAI | Adult Attachment Interview |
| ABLES | Adult Blood Lead Epidemiology and Surveillance program |
| pseudo-osteomalacia | Rachitic softening of bone. (05 Mar 2000) |
|---|---|
| senile osteomalacia | Osteoporosis in the aged. (05 Mar 2000) |
| due date | The estimated calendar date when a baby will be born, the date the baby is due to be born. It is also called the estimated date of confinement (EDC). (12 Dec 1998) |
| dystonia, focal, due to blepharospasm | The second most common focal dystonia, the involuntary, forcible closure of the eyelids. The first symptoms may be uncontrollable blinking. Only one eye may be affected initially, but eventually both eyes are usually involved. The spasms may leave the eyelids completely closed causing functional blindness even though the eyes and vision are normal. (12 Dec 1998) |
| dystonia, focal, due to torticollis | Spasmodic torticollis, or torticollis, is the most common of the focal dystonias. In torticollis, the muscles in the neck that control the position of the head are affected, causing the head to twist and turn to one side. In addition, the head may be pulled forward or backward. (12 Dec 1998) |
| infantile osteomalacia | <rheumatology, orthopaedics> A condition caused by deficiency of vitamin D, especially in infancy and childhood, with disturbance of normal ossification. The disease is marked by bending and distortion of the bones under muscular action, by the formation of nodular enlargements on the ends and sides of the bones, by delayed closure of the fontanelles, pain in the muscles and sweating of the head. Vitamin D and sunlight together with an adequate diet are curative, provided that the parathyroid glands are functioning properly. Origin: Gr. Rhachitis = a spinal complaint (18 Nov 1997) |
| osteomalacia | <pathology> A condition marked by softening of the bones (due to impaired mineralisation, with excess accumulation of osteoid), with pain, tenderness, muscular weakness, anorexia and loss of weight, resulting from deficiency of vitamin D and calcium. Origin: Gr. Malakia = softness (18 Nov 1997) |
| thrombotic disease due to protein c deficiency | Protein C is a protein in plasma that enters into the cascade of biochemical events leading to the formation of a clot. Deficiency of protein c results in thrombotic (clotting) disease and excess platelets with recurrent thrombophlebitis (inflammation of the vein that occurs when a clot forms). The clot can break loose and travel through the blood stream (thromboembolism) to the lungs causing a pulmonary embolism, brain causing a stroke (cerebrovascular accident), heart causing an early heart attack, skin causing what in the newborn is called neonatal purpura fulminans, the adrenal gland causing haemorrhage with abdominal pain, abnormally low blood pressure (hypotension), and salt loss. Protein c deficiency is due to possession of one gene (heterozygosity) in chromosome band 2q13-14. The possession of two such genes (homozygosity) is usually lethal. (12 Dec 1998) |
| malabsorption | <gastroenterology> Impaired intestinal absorption of nutrients. (18 Nov 1997) |
| malabsorption syndrome | <syndrome> A variety of conditions in which digestion and absorption in the small intestine are impaired. Multiple causes including lymphoma, amyloid and other infiltrations, Crohn's disease, gluten sensitive enteropathy and the sprue syndrome in which the villi atrophy for unknown reasons. (18 Nov 1997) |
| malabsorption syndromes | General term for syndromes of malnutrition due to failure of normal intestinal absorption of nutrients. (12 Dec 1998) |
| methionine malabsorption syndrome | <syndrome> An inherited disorder in which there is an inability to absorb l-methionine from the gut. (05 Mar 2000) |
| intestinal malabsorption | <gastroenterology> The inadequate absorption of nutrients from the small intestine. This can result in loss of weight and abnormal appearing stools. Malabsorption can be caused by lesions of the small intestine, amyloidosis, lack of digestive enzymes (for example lactose intolerance) or bile salts or surgical operations. (10 Jan 1998) |
| adult | A living organism which has attained full growth or maturity. Origin: L. Adultus = grown up (18 Nov 1997) |
| adult lactase deficiency | Onset of lactase deficiency, with resulting milk intolerance and malabsorption, in adulthood. Inherited forms may not be manifested until adulthood; any process that damages the intestinal lining cells can cause lactase deficiency in adults. (05 Mar 2000) |
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