| AHC | Albright's Hereditary Osteodystrophy |
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| AHO | Albright's Hereditary Osteodystrophy |
| AHO | Albright hereditary osteodystrophy |
| DOOR | deafness, onycho-osteodystrophy, mental retardation [syndrome] |
| RO | radiation oncology; radiation output; ratio of; relative odds; renal osteodystrophy; reverse osmosis... |
| AHO | Albright hereditary osteodystrophy |
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| MAS | McCune Albright syndrome |
| ROD | Renal osteodystrophy |
| CHED | Congenital Hereditary Endothelial Dystrophy |
| HANE | Hereditary Angio Neurotic Edema |
| Albright's hereditary osteodystrophy | An inherited form of hyperparathyroidism associated with ectopic calcification and ossification and skeletal defects, notably the small fourth metacarpals, but intelligence is normal. There are dominant, recessive and X-linked forms. See: pseudohypoparathyroidism. Synonym: Albright's syndrome. (05 Mar 2000) |
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| renal osteodystrophy | Generalised changes in the bone which resemble osteomalacia and rickets, occurring in those with chronic renal failure. (27 Sep 1997) |
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| chondro-osteodystrophy | Term used for a group of disorders of bone and cartilage which includes Morquio syndrome and similar conditions. Synonym: osteochondrodystrophia deformans, osteochondrodystrophy. (05 Mar 2000) |
| congenital renal osteodystrophy | <radiology> Tubular form of renal osteodystrophy, vitamin D-resistant rickets, Fanconi syndrome, renal tubular acidosis (12 Dec 1998) |
| osteodystrophy | <pathology> Defective bone formation. (18 Nov 1997) |
| Albright, Fuller | <person> Physician, 1900-1969. See: Albright's disease, Albright's syndrome, Albright's hereditary osteodystrophy, Forbes-Albright syndrome, McCune-Albright syndrome. (05 Mar 2000) |
| Albright's disease | <syndrome> The abnormal development of multiple bones, hormonal disorder and brownish skin lesions. (27 Sep 1997) |
| Albright's syndrome | <syndrome> A condition of cystic bone growth that results from abnormal bone development. May occur with bone lesions, skin pigmentation and endocrine abnormalities. See: McCune-Albright syndrome. (27 Sep 1997) |
| McCune-Albright syndrome | <syndrome> The abnormal development of multiple bones, hormonal disorder and brownish skin lesions. (27 Sep 1997) |
| Forbes-Albright syndrome | <endocrinology, syndrome> Pituitary tumour in a patient without acromegaly, which secretes excessive amounts of prolactin (LTH) and produces persistent lactation. (05 Mar 2000) |
| angioedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
| angioneurotic oedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
| canine hereditary blindness | An autosomal dominant condition seen in dogs of the collie and several other breeds. (05 Mar 2000) |
| colourectal neoplasms, hereditary nonpolyposis | A syndrome characterised by autosomal dominant inheritance, a low mean age (41 years) for occurrence of colon cancer, and a marked increase in the proportion of tumours in the proximal colon. (12 Dec 1998) |
| corneal dystrophies, hereditary | Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect. (12 Dec 1998) |
| hereditary | <genetics> Transferred via genes from parent to child. (16 Dec 1997) |
| Albright's hereditary osteodystrophy, syndrome |
see pseudohypoparathyroidism and see under syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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