| HOA | Hypertrophic Osteoarthropathy |
|---|---|
| HOA | hip osteoarthritis; hypertrophic osteoarthropathy |
| HPO | high-presure oxygen; hydroperoxide; hydrophilic ointment; hypertrophic pulmonary osteoarthropathy |
| HPOA | hypertrophic pulmonary osteoarthropathy |
| SHO | secondary hypertrophic osteoarthropathy; Senior House Officer |
| HOA | Hypertrophic osteoarthropathy |
|---|---|
| HPOA | Hypertrophic pulmonary osteoarthropathy |
| DRO | Differential Reinforcement of Other Behaviour |
| MOTT | Mycobacteria Other Than Tuberculosis |
| OND | Other Neurological Diseases |
| hypertrophic osteoarthropathy | <radiology> Pulmonary, malignancy (bronchogenic carcinoma, lymphoma, metastasis), abscess, COPD / bronchiectasis, pleural, pleural fibroma (highest incidence of HOA, tho' rare itself), mesothelioma, cardiac, cyanotic congenital heart disease, GI, inflammatory disease (Crohn, UC), malabsorption (dysentery, lue, cirrhosis), ** causes symmetrical periosteal reaction (12 Dec 1998) |
|---|---|
| osteoarthropathy, primary hypertrophic | A conditioned chiefly characterised by thickening of the skin of the head and distal extremities, deep folds and furrows of the skin of the forehead, cheeks, and scalp, seborrhoea, hyperhidrosis, periostosis of the long bones, digital clubbing, and spadelike enlargement of the hands and feet. It is more prevalent in the male, and is usually first evident during adolescence. It is believed to be inherited as an autosomal dominant trait. (12 Dec 1998) |
| osteoarthropathy, secondary hypertrophic | Symmetrical osteitis of the four limbs, chiefly localised to the phalanges and the terminal epiphyses of the long bones of the forearm and leg, sometimes extending to the proximal ends of the limbs and the flat bones, and accompanied by dorsal kyphosis and joint involvement. It is often secondary to chronic conditions of the lungs and heart. (12 Dec 1998) |
| other-directed | Pertaining to a person readily influenced by the attitudes of others. (05 Mar 2000) |
| transferases (other substituted phosphate groups) | <enzyme> A class of enzymes that transfers substituted phosphate groups. Registry number: EC 2.7.8 (12 Dec 1998) |
| pneumogenic osteoarthropathy | hypertrophic pulmonary osteoarthropathy |
| pulmonary osteoarthropathy | hypertrophic pulmonary osteoarthropathy |
| osteoarthropathy | <orthopaedics, pathology, rheumatology> A condition which describes the broadening or thickening of the tips of the fingers (and toes) with increased lengthwise curvature of the nail and a decrease in the angle normally seen between the cuticle and the fingernail. Often this finding on physical examination can be quite subtle and easily overlooked. Clubbing may be seen in a wide variety of conditions---most of which result in a decrease in blood oxygen. Examples include: tetralogy of Fallot, transposition of the great vessels, atrial myxomas, cystic fibrosis, emphysema, lung cancer, tuberculosis, cystic fibrosis, bronchiectasis, Hodgkin's disease, cirrhosis, chronic active hepatitis and Crohn's disease. This finding will generally provoke a more detailed patient evaluation. Origin: Gr. Pathos = disease (27 Sep 1997) |
| cardiomyopathy, hypertrophic | A myocardial disease characterised by hypertrophy, involving mainly the interventricular septum, interfering with left ventricular emptying. (12 Dec 1998) |
| gastritis, hypertrophic | Gastritis with hypertrophy of gastric mucosa folds. Symptoms include vomiting, diarrhoea, weight loss, excessive mucus secretion, and hypoproteinaemia. (12 Dec 1998) |
| chronic hypertrophic vulvitis | Swelling of the vulval tissues due to lymphatic obstruction; in some cases it may be caused by filariasis, with induration or ulceration of the skin. Synonym: elephantiasis vulvae. (05 Mar 2000) |
| chronic interstitial hypertrophic neuropathy | dejerine-Sottas disease |
| cicatrix, hypertrophic | An elevated scar, resembling a keloid, but which does not spread into surrounding tissues. It is formed by enlargement and overgrowth of cicatricial tissue and regresses spontaneously. (12 Dec 1998) |
| progressive hypertrophic polyneuropathy | A familial type of demyelinating sensorimotor polyneuropathy that begins in early childhood and is slowly progressive; clinically characterised by foot pain and paresthesias, followed by symmetrical weakness and wasting of the distal limbs; one of the causes of stork legs; patients are wheelchair bound at an early age; peripheral nerves are palpably enlarged and non-tender; pathologically, onion bulb formation is seen in the nerves: whorls of overlapping, intertwined Schwann cell processes that encircle bare axons; usually autosomal recessive inheritance. Synonym: Dejerine's disease, progressive hypertrophic polyneuropathy. (05 Mar 2000) |
| hereditary hypertrophic neuropathy | dejerine-Sottas disease |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|