| LCL | Levinthal-Coles-Lillie [body]; lower confidence limit; lower control limit; lymphoblastoid cell line... |
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| LLSB | left lower scapular border; left lower sternal border |
| LRI | lamina rara interna; lower respiratory [tract] illness; lower respiratory [tract] infection; lymphoc... |
| LRTI | lower respiratory tract illness; lower respiratory tract infection |
| RLL | right lobe of liver; right lower limb; right lower lobe |
| lower segment cesarian section | A Cesarian section in which the surgical incision (cut) is made in the lower segment of the uterus. (12 Dec 1998) |
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| Lower's ring | One of four fibrous rings that surround atrioventricular and arterial orifices of the heart, providing attachment for the valve leaflets and maintaining patency of the orifice. As part of the fibrous skeleton of the heart, the fibrous rings also provide origin and insertion for the myocardium. Synonym: annulus fibrosus cordis, annulus fibrosus, coronary tendon, fibrous ring, Lower's ring. (05 Mar 2000) |
| Lower's tubercle | The slight projection on the wall of the right atrium between the orifices of the venae cavae. Synonym: tuberculum intervenosum, Lower's tubercle. (05 Mar 2000) |
| lower uterine segment | The inferior portion or isthmus of the uterus, the lower extremity of which joins with the cervical canal and, during pregnancy, expands to become the lower part of the uterine cavity. (05 Mar 2000) |
| lower uterine segment cesarean section | A cesarean section in which the uterus is entered in its lower segment by a transperitoneal approach. (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) |
| congenital absence of pulmonary valve | <radiology> BIG central pulmonary arteries, big RV (12 Dec 1998) |