| eustachian valve | An endocardial fold extending from the anterior inferior margin of the inferior vena cava to the anterior part of the limbus fossa ovalis. Synonym: valvula venae cavae inferioris, caval valve, eustachian valve, sylvian valve. (05 Mar 2000) |
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| Krause's valve | A small fold in the interior of the lacrimal sac at its junction with the lacrimal duct. Synonym: Krause's valve. (05 Mar 2000) |
| floppy valve syndrome | <syndrome> Retrograde slippage of degenerating mitral or tricuspid valve leaflets into the valve's orifice beyond the point of closure during systole of the left ventricle; a feature of Barlow's syndrome. (05 Mar 2000) |
| frenulum of ileocaecal valve | A fold, more evident in cadavers, running from the junction of the two commissures of the ileocaecal valve on either side along the inner wall of the caecocolic junction. Synonym: frenulum valvae ileocaecalis, frenulum of Morgagni, Morgagni's frenum, Morgagni's retinaculum. (05 Mar 2000) |
| left atrioventricular valve | <anatomy, cardiology> The heart valve that divides the left atrium and left ventricle. During left atrial contraction, the mitral valve opens to allow blood to flow into the left ventricle. Upon closure, the mitral valve prohibits the regurgitation of blood back into the left atrium. The mitral valve is the only heart valve that has only 2 valve cusps (all others have 3). (13 Nov 1997) |
| lunula of semilunar valve | The free border of a semilunar valve at each side of the nodulus valvulae semilunaris. Synonym: lunula valvulae semilunaris. (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) |
| congenital | <embryology> Existing at and usually before, birth, referring to conditions that are present at birth, regardless of their causation. Origin: L. Congenitus = born together (18 Nov 1997) |