| sER | smooth endoplasmic reticulum |
|---|---|
| SM | Master of Science; sadomasochism; self-monitoring; silicon microphysiometer; simple mastectomy; skim... |
| SMAF | smooth muscle activating factor; specific macrophage arming factor |
| SMC | Scientific Manpower Commission; smooth muscle cell; somatomedin C; succinylmonocholine |
| SMCA | smooth muscle contracting agent; suckling mouse cataract agent |
| ischemic muscular atrophy | See: Volkmann's contracture. (05 Mar 2000) |
|---|---|
| electro-muscular | <physiology> Pertaining the reaction (contraction) of the muscles under electricity, or their sensibility to it. Source: Websters Dictionary (01 Mar 1998) |
| Emery-Dreifuss muscular dystrophy | A generally benign type of muscular dystrophy, with onset in childhood or early adulthood. Weakness begins with the pectoral girdle and proximal upper extremity muscles and spreads to the pelvic girdle and distal lower extremity muscles. Contractures of the elbow, flexors, neck flexors, and calf muscles often occur; muscle pseudohypertrophy and mental retardation do not occur. A cardiomyopathy is common. An X-linked inherited disorder, nonallelic to Duchenne's muscular dystrophy. (05 Mar 2000) |
| juvenile muscular atrophy | Slowly progressive proximal muscular weakness and wasting, beginning in childhood, caused by degeneration of motor neurons in the anterior horns of the spinal cord; onset usually between 2 and 17 years of age; usually autosomal recessive inheritance. Synonym: juvenile muscular atrophy, Kugelberg-Welander disease, Wohlfart-Kugelberg-Welander disease. (05 Mar 2000) |
| juvenile spinal muscular atrophy | Slowly progressive proximal muscular weakness and wasting, beginning in childhood, caused by degeneration of motor neurons in the anterior horns of the spinal cord; onset usually between 2 and 17 years of age; usually autosomal recessive inheritance. Synonym: juvenile muscular atrophy, Kugelberg-Welander disease, Wohlfart-Kugelberg-Welander disease. (05 Mar 2000) |
| facioscapulohumeral muscular dystrophy | A relatively benign type of muscular dystrophy commencing in childhood and slowly progressive; characterised by wasting and weakness, sometimes asymmetrical, mainly of the muscles of the face, shoulder girdle, and arms; autosomal dominant inheritance. Synonym: facioscapulohumeral atrophy, Landouzy-Dejerine dystrophy. (05 Mar 2000) |
| familial spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| Leyden-Mobius 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-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) |
| longitudinal layer of muscular coat | The outer, longitudinal layer of the smooth muscle of the muscular coat. Nomina Anatomica lists longitudinal layers of muscular coats (stratum longitudinale tunicae muscularis...) of the following: 1) colon (... Coli ); 2) rectum (... Recti ); 3) small intestine (... Intestini tenuis ); 4) stomach (... Gastrici ). Synonym: stratum longitudinale tunicae muscularis gastricae, stratum longitudinale tunicae muscularis. (05 Mar 2000) |
| longitudinal layers of muscular tunics | See: longitudinal layer of muscular coat. (05 Mar 2000) |
| anal sphincter | See: external anal sphincter, internal anal sphincter. (05 Mar 2000) |
| anatomical sphincter | An accumulation of muscular circular fibres or specially arranged oblique fibres the function of which is to reduce partially or totally the lumen of a tube, the orifice of an organ, or the cavity of a viscus; the closing component of a pylorus. (05 Mar 2000) |
| annular sphincter | A short thickening of circular muscular fibres, similar to a ring; a ring-shaped sphincter as opposed to a segmental sphincter. (05 Mar 2000) |
| antral sphincter | Angular sphincter, thickening of the circular muscular layer forming a proposed intermediate sphincter at the level of the angular notch of the stomach. While the thickening of the circular muscle may indicate the commencement of the pyloric antrum, true functional sphincteric activity distinct from the other peristaltic contractions of the stomach is not observed although some of these may in fact temporarily close off the antrum from the remainder of the stomach lumen. Synonym: antral sphincter, midgastric transverse sphincter, sphincter antri, sphincter intermedius, sphincter of antrum, sphincter of gastric antrum. (05 Mar 2000) |