| aVL | unipolar limb lead on the left arm in electrocardiography |
|---|---|
| aVR | unipolar limb lead on the right arm in electrocardiography |
| CLH | chronic lobular hepatitis; cleft limb-heart [syndrome]; corpus luteum hormone; cutaneous lymphoid hy... |
| cTAL | cortical thick ascending limb |
| ILD | interstitial lung disease; intraoperative localization device; ischemic leg disease; ischemic limb d... |
| lateral limb | Limb or leg-like portion of a structure, farthest from midline. Synonym: crus laterale, lateral limb. (05 Mar 2000) |
|---|---|
| lateral surface of lower limb | The lateral surface of the inferior limb. Synonym: facies lateralis membri inferioris. (05 Mar 2000) |
| limb | A leg or arm. A branch of a tree. The upper, free, spreading portion of a corolla or perianth that is connate at the base. (09 Oct 1997) |
| limb bud | The limbs of vertebrates start as outpushings of mesenchyme surrounded by a simple epithelium. The distal region is referred to as the progress zone. There has been extensive study of positional information within the limb bud that determines, for example: the proximal distal pattern of bone development and the anterior posterior specification of digits. (18 Nov 1997) |
| limb-girdle muscular dystrophy | One of the less well-defined types of muscular dystrophy, probably heterogenous in nature. Onset usually in childhood or early adulthood and both sexes affected. Characterised by weakness and wasting, usually symmetrical, of the pelvic girdle muscles, the shoulder girdle muscles, or both, but not the facial muscles. Muscle pseudohypertrophy, heart involvement, and mental retardation are absent. Variable inheritance. Synonym: Leyden-Mobius muscular dystrophy, pelvofemoral muscular dystrophy, scapulohumeral muscular dystrophy. (05 Mar 2000) |
| limb-kinetic apraxia | An inability to make movements or to use objects for the purpose intended. Synonym: cortical apraxia, innervation apraxia, limb-kinetic apraxia. (05 Mar 2000) |
| limb lead | One of the three standard leads (leads I, II, III) or one of the unipolar limb lead's (aVR, aVL, aVF). (05 Mar 2000) |
| limb myokymia | Myokymia present in one or more limbs; various causes, one of the more common being prior plexus radiation. (05 Mar 2000) |
| limb of helix | A transverse ridge continuing backward from the helix of the auricle, dividing the concha into an upper portion (cymba) and a lower portion (cavity of concha). Synonym: crus helicis, crista helicis, limb of helix. (05 Mar 2000) |
| lower limb | The hip, thigh, leg, ankle, and foot. Synonym: membrum inferius, inferior limb, lower extremity, pelvic limb. (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) |