| CBPS | congenital bilateral perisylvian syndrome |
|---|---|
| CCA | cephalin cholesterol antigen; chick cell agglutination; chimpanzee coryza agent; choriocarcinoma; ci... |
| CCHD | cyanotic congenital heart disease |
| CCHS | congenital central hypoventilation syndrome |
| CCVM | congenital cardiovascular malformation |
| lens nucleus, crystalline | The core of the crystalline lens, surrounded by the cortex. (12 Dec 1998) |
|---|---|
| lens pits | The paired depressions formed in the superficial ectoderm of the embryonic head as the lens placodes sink in toward the optic cup; the external openings of the pit's are closed as the lens vesicles are formed. (05 Mar 2000) |
| lens placodes | Paired ectodermal placode's that become invaginated to form the embryonic lens vesicles. Synonym: optic placodes. (05 Mar 2000) |
| lens, simple | <microscopy> A glass disk ground and polished with a spherical figure on one side and a plano, concave, or convex configuration on the other side. (05 Aug 1998) |
| lens stars | Congenital cataracts with opacities along the suture lines of the lens; may be anterior or posterior or both. (05 Mar 2000) |
| lens subluxation | Incomplete rupture of the zonule with the displaced lens remaining behind the pupil. In dislocation, or complete rupture, the lens is displaced forward into the anterior chamber or backward into the vitreous body. When congenital, this condition is known as ectopia lentis. (12 Dec 1998) |
| lens sutures | 9 to 12 faint lines on the anterior and posterior surfaces of the lens that radiate from the poles toward the equator; they mark the lines along which the ends of lens fibres abut. Synonym: lens stars, lens sutures. (05 Mar 2000) |
| lens vesicle | In the embryo, the ectodermal invagination that forms opposite the optic cup; it is the primordium of the lens of the eye. Synonym: lenticular vesicle. (05 Mar 2000) |
| lighthouse lens | <physics> A lens built up, progressively, in zones or steps, each zone with its own individual radius. Considerable spherical correction is attained, and the weight of the lens is greatly reduced. Fresnel lenses were originally designed for lighthouses but they are now attainable for small spotlights, automobile headlights, and similar uses. (05 Aug 1998) |
| 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) |