| CLE | centrilobular emphysema; continuous lumbar epidural [anesthesia] |
|---|---|
| COPE | chronic obstructive pulmonary emphysema |
| CPE | cardiac pulmonary edema; chronic pulmonary emphysema; clinical progress exercise; compensation, pens... |
| dif-PIPE | diffuse persistent interstitial pulmonary emphysema |
| EAI | Emphysema Anonymous, Inc.; erythrocyte antibody inhibition |
| interlobular emphysema | Interstitial emphysema in the connective tissue septa between the pulmonary lobules. (05 Mar 2000) |
|---|---|
| interstitial emphysema | Presence of air in the pulmonary tissues consequent upon rupture of the air cells, presence of air or gas in the connective tissue. (05 Mar 2000) |
| intestinal emphysema | A condition characterised by the presence of thin-walled, gas-containing cysts in the wall of the intestines. The lesions may be subserosal or submucosal. (12 Dec 1998) |
| irregular emphysema | Emphysema that shows no consistent relationship to any portion of the acinus; always associated with fibrosis. (05 Mar 2000) |
| ectatic emphysema | Obstructive airway disease with areas of dilatation of alveoli acini. Seen primarily in association with inherited deficiency of alpha-1 protease inhibitor. See: panlobular emphysema. (05 Mar 2000) |
| emphysema | <chest medicine> A pathological accumulation of air in tissues or organs, applied especially to such a condition of the lungs. (18 Nov 1997) |
| familial emphysema | Emphysema inherited in association with severe alpha-1 antitrypsin deficiency. It may occur as an isolated feature or with cutis laxa and haemolytic anaemia. (05 Mar 2000) |
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia, haemolytic, congenital | Haemolytic anaemia due to various intrinsic defects of the erythrocyte. (12 Dec 1998) |
| anaemia, haemolytic, congenital nonspherocytic | Any one of a group of congenital haemolytic anaemias in which there is no abnormal haemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated. (12 Dec 1998) |
| bovine congenital ataxia | An autosomal recessive ataxia seen in several European breeds of cattle. (05 Mar 2000) |
| bullous congenital ichthyosiform erythroderma | Diffusely red, eroded skin at birth, with subsequent scaling, tending to improve in later life, characterised by generalised epidermolytic hyperkeratosis and autosomal dominant inheritance. See: epidermolytic hyperkeratosis. Synonym: generalised epidermolytic hyperkeratosis, ichthyismus hystrix, ichthyosis hystrix. (05 Mar 2000) |
| pain insensitivity, congenital | Absence of sensibility to pain or inability to feel pain. The condition is present at birth. (12 Dec 1998) |
| rubella syndrome, congenital | Transplacental infection of the foetus with rubella usually in the first trimester of pregnancy, as a consequence of maternal infection, resulting in various developmental abnormalities in the newborn infant. They include cardiac and ocular lesions, deafness, microcephaly, mental retardation, and generalised growth retardation. (12 Dec 1998) |