| PL | palmaris longus; pancreatic lipase; perception of light; peroneus longus; phospholipase; phospholipi... |
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| PLB | parietal lobe battery; phospholamban; phospholipase B; porous layer bead |
| PTLC | precipitation thin-layer chromatography |
| Rf | in paper or thin-layer chromatography, the distance that a spot of a substance has moved from the po... |
| Rst | in paper or thin layer chromatography, the distance that a spot of a substance has moved, relative t... |
| muscular sense | The sensation felt in muscle when it is contracting; awareness of movement or activity in muscles or joints; sense of position or movement mediated in large part by the posterior columns and medial lemniscus. See: bathyesthesia. Synonym: deep sensibility, kinesthetic sense, mesoblastic sensibility, muscular sense, myoesthesis, myoesthesia. Origin: G. Mys, muscle, + aisthesis, sensation (05 Mar 2000) |
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| muscular subaortic stenosis | <cardiology> A congenital heart disease that results in abnormal thickening of the ventricular septum and left ventricular wall. Enlargement of the ventricular septum can result in ventricular outflow obstruction (subaortic stenosis) and eventual cardiomyopathy. (27 Sep 1997) |
| muscular substance of prostate | The smooth muscle in the stroma of the prostate. Synonym: substantia muscularis prostatae, musculus prostaticus. (05 Mar 2000) |
| muscular system | All the muscles of the body collectively. (05 Mar 2000) |
| muscular tissue | A tissue characterised by the ability to contract upon stimulation; its three varieties are skeletal, cardiac, and smooth. See: muscle. Synonym: flesh. (05 Mar 2000) |
| muscular triangle | The triangle bounded by the sternocleidomastoid muscle, the superior belly of the omohyoid muscle, and the anterior midline of the neck; the infrahyoid muscles occupy most of it. Synonym: trigonum musculare, trigonum omotracheale, inferior carotid triangle, omotracheal triangle, tracheal triangle. (05 Mar 2000) |
| muscular trophoneurosis | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
| muscular tunic of gallbladder | Muscular tunic of the gallbladder, consisting of layers of smooth muscle fibres coursing in various directions immediately external to the mucosa of the gallbladder. (05 Mar 2000) |
| muscular tunics | See: muscular coat. (05 Mar 2000) |
| progressive infantile 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) |
| progressive muscular atrophy | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
| progressive muscular dystrophy | A form of progressive muscular atrophy in which the disease begins in the muscle and not in the spinal centres. Synonym: Erb atrophy, idiopathic muscular atrophy. (05 Mar 2000) |
| progressive spinal muscular atrophy | One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of the spinal cord, manifested as progressive, often symmetrical, weakness and wasting, typically beginning in the distal portions of the limbs, particularly in the upper extremities, and spreading proximally; fasciculation potentials are often present, but evidence of corticospinal tract disease (e.g., increased deep tendon reflexes, Babinski sign) is not. (05 Mar 2000) |
| scapulohumeral 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) |
| pseudohypertrophic muscular dystrophy | The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females). Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy. (05 Mar 2000) |