| SMD | senile macular degeneration; spondylometaphyseal dysplasia; submanubrial dullness |
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| CRD | carbohydrate-recognition domain; chronic renal disease; chronic respiratory disease; child restraint... |
| RD | radial deviation; radiology department; rate difference; Raynaud disease; reaction of degeneration; ... |
| SCD | scleroderma; service-connected disability; sickle-cell disease; spinocerebellar degeneration; subacu... |
| CME | cervical mediastinal exploration; continuing medical education; Council on Medical Education; crude ... |
| macular fasciculus | The collection of fibres in the optic nerve directly connected with the macula lutea. Synonym: fasciculus macularis. (05 Mar 2000) |
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| macular leprosy | A form of tuberculoid leprosy in which the lesions are small, hairless, and dry, and are erythematous in light skin and hypopigmented or copper-coloured in dark skin. (05 Mar 2000) |
| macular oedema, cystoid | Macular degeneration characterised by oedema and cystic spaces which may lead to a macular depression or hole. (12 Dec 1998) |
| macular retinopathy | Any pathological condition of the macula lutea. Synonym: macular retinopathy. (05 Mar 2000) |
| macular syphilid | Usually the first eruption of syphilis, occurring 6 to 12 weeks after the initial lesion. Synonym: erythematous syphilid, macular syphilid. (05 Mar 2000) |
| cystoid macular oedema | Oedema of the posterior pole of the eye secondary to abnormal permeability of capillaries of the central sensory retina. (05 Mar 2000) |
| primary idiopathic macular atrophy | Atrophoderma in which the skin becomes bag like and wrinkled. Synonym: atrophia maculosa varioliformis cutis, atrophoderma maculatum, macular atrophy, primary idiopathic macular atrophy, primary macular atrophy of skin. Origin: G. Anetos, relaxed, + derma, skin (05 Mar 2000) |
| primary macular atrophy of skin | Atrophoderma in which the skin becomes bag like and wrinkled. Synonym: atrophia maculosa varioliformis cutis, atrophoderma maculatum, macular atrophy, primary idiopathic macular atrophy, primary macular atrophy of skin. Origin: G. Anetos, relaxed, + derma, skin (05 Mar 2000) |
| superior macular arteriole | Origin, central artery of retina; distribution, upper part of macula. Synonym: arteriola macularis superior. (05 Mar 2000) |
| superior macular venule | A small tributary of the central vein of the retina that drains the upper part of the macula. Synonym: venula macularis superior. (05 Mar 2000) |
| inferior macular arteriole | Origin, central artery of retina; distribution, inferior part of macula. Synonym: arteriola macularis inferior. (05 Mar 2000) |
| inferior macular venule | A small tributary of the central vein of the retina that drains the lower part of the macula. Synonym: venula macularis inferior. (05 Mar 2000) |
| 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) |
| 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) |