| CMS | children's medical services; Christian Medical Society; chronic myelodysplastic syndrome; chromosome... |
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| COD-MD | cerebro-ocular dysplasia-muscular dystrophy [syndrome] |
| CSMA | chronic spinal muscular atrophy |
| CXMD | canine X-linked muscular dystrophy |
| DMD | disease-modifying drug; Doctor of Dental Medicine; Duchenne muscular dystrophy; dystonia musculorum ... |
| muscular layer of mucosa | The thin layer of smooth muscle found in most parts of the digestive tube located outside the lamina propria mucosae and adjacent to the tela submucosa. Synonym: lamina muscularis mucosae, muscular layer of mucosa. (05 Mar 2000) |
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| muscular movement | Movement caused by the contraction of the myofibrils of the muscle cells. (05 Mar 2000) |
| muscular part of interventricular septum of heart | The thick muscular portion which comprises most of the interventricular septum of the heart. Synonym: pars muscularis septi interventricularis cordis, septum musculare ventriculorum. (05 Mar 2000) |
| muscular process of arytenoid cartilage | The blunt lateral projection of the arytenoid cartilage giving attachment to the lateral and posterior cricoarytenoid muscles of the larynx. Synonym: processus muscularis cartilaginis arytenoidei. (05 Mar 2000) |
| muscular pulley | A fibrous loop through which the tendon of a muscle passes; the intermediate tendon of the digastric and omohyoid muscles pass through such a trochlea. Synonym: trochlea muscularis. (05 Mar 2000) |
| muscular reflex | Tonic contraction of the muscles in response to a stretching force, due to stimulation of muscle proprioceptors. Synonym: Liddell-Sherrington reflex, muscular reflex, stretch reflex. (05 Mar 2000) |
| muscular rheumatism | <pathology> A disorder characterised by muscle pain, stiffness and easy fatigability. The cause is unknown and an estimated 3 million Americans are affected. (27 Sep 1997) |
| 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) |
| 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) |
| 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) |
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| 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) |
Synonyms : Dystrophies, Oculopharyngeal Muscular, Dystrophy, Oculopharyngeal Muscular, Muscular Dystrophies, Oculopharyngeal, Oculopharyngeal Muscular Dystrophies, Oculopharyngeal Muscular Dystrophy
| muscular dystrophy |
a rare genetic disorder in which muscles degenerate gradually and strength is lost
출처: www.american-depot.com/services/resources_gl_m.asp
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| muscular |
severe myalgia or creatine phosphokinase level at least twice the upper limit of normal
출처: www.cdc.gov/epo/dphsi/print/toxic_shock_syndrome_c...
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| muscular |
abnormal modifications of a muscle, that becomes less voluminous, shorter, and harder.
출처: www.genethon.fr/php/layout.php
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| muscular dystrophy |
muscle involvement characterised by progressive volume loss and weakening of certain groups of muscles.
출처: www.genethon.fr/php/layout.php
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| muscular dystrophy |
is a broad term that describes a genetic (inherited) disorder of the muscles. MD causes the muscles in the body to become very weak. The muscles break down and are replaced with fatty deposits over time. The most common form of MD is called Duchenne muscular dystrophy (DMD).
출처: www.uchicagokidshospital.org/online-library/conten...
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