| TLC | tender loving care; thin-layer chromatography; total L-chain concentration; total lung capacity; tot... |
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| TLE | temporal lobe epilepsy; thin-layer electrophoresis; total lipid extract |
| TVL | tenth value layer; tunica vasculosa lentis |
| DMD | Duchenne type Muscular Dystrophy; 악성형 Duchenne형 근이영양증 |
| FMD | Fibro-Muscular Dysplasia |
| electro-muscular | <physiology> Pertaining the reaction (contraction) of the muscles under electricity, or their sensibility to it. Source: Websters Dictionary (01 Mar 1998) |
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| 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 layers of muscular tunics | See: longitudinal layer of muscular coat. (05 Mar 2000) |
| Abbott's tube | A tube with two lumens, one ending in a small collapsible balloon and the other in a metallic tip with numerous perforations; used for intestinal decompression. Synonym: Abbott's tube. (05 Mar 2000) |
| abdominal ostium of uterine tube | The fimbriated or ovarian extremity of an oviduct. Synonym: ostium abdominale tubae uterinae. (05 Mar 2000) |
| air cells of auditory tube | Occasional small air cells in the inferior wall of the auditory tube, near the tympanic orifice, communicating with the tympanic cavity. Synonym: cellulae pneumaticae tubae auditivae, air cells of auditory tube. (05 Mar 2000) |
| air tube | The trachea, or a bronchus or any of its branches conveying air to the lungs. (05 Mar 2000) |
| alar lamina of neural tube | The dorsal division of the lateral walls of the neural tube in the embryo; it gives rise to neurons relaying afferent impulses to higher centres; in the adult such neurons compose the sensory nuclei of the spinal cord and brainstem. Synonym: lamina alaris, alar plate of neural tube, dorsolateral plate of neural tube, lamina dorsalis, wing plate. (05 Mar 2000) |
| alar plate of neural tube | The dorsal division of the lateral walls of the neural tube in the embryo; it gives rise to neurons relaying afferent impulses to higher centres; in the adult such neurons compose the sensory nuclei of the spinal cord and brainstem. Synonym: lamina alaris, alar plate of neural tube, dorsolateral plate of neural tube, lamina dorsalis, wing plate. (05 Mar 2000) |