| NM | 1) Neuro-Muscular 2) Neo-Mycin |
|---|---|
| VSD | Ventricular Septal Defect ? Types of VSD 1. Subpulmonic(=... |
| BDM | Becker's muscular dystrophy |
| BMD | Becker's muscular dystrophy; Boehringer Mannheim Diagnostics; bone marrow depression; bone mineral d... |
| CASMD | congenital atonic sclerotic muscular dystrophy |
muscularis mucosae (근육 층, 점막 근육 판, 점막근 판
| muscular coat of small intestine | Muscular layer of the wall of the small intestine. Synonym: tunica muscularis intestini tenuis. (05 Mar 2000) |
|---|---|
| muscular coat of stomach | Muscular tunic of the stomach, consisting of smooth muscles arranged in three fairly well defined layers: an outer longitudinal layer, continuous with that of the oesophagus but dividing at the cardia into two bands which run along the greater and lesser curvatures, leaving the middle areas of the anterior and posterior walls devoid of longitudinal fibres, and then coalescing in the pyloric region into a complete layer which is continuous with the longitudinal coat of the duodenum. The middle circular layer is most complete and strongest, continuous with the circular layer of the oesophagus at the cardia; it thickens progressively toward the pylorus, ultimately forming the muscular ring of the pyloric sphincter. The inner, oblique layer is unique to the stomach and is most strongly developed in the fundic region and absent along the lesser curvature. This absence contributes to the formation of the "gastric canal." See: oblique fibres of stomach. Synonym: tunica muscularis gastrica, tunica muscularis ventriculi. (05 Mar 2000) |
| muscular coat of trachea | Muscular layer of the tracheal wall. Synonym: tunica muscularis tracheae. (05 Mar 2000) |
| muscular coat of ureter | Muscular layer of the ureteric wall. Synonym: tunica muscularis ureteris. (05 Mar 2000) |
| muscular coat of urinary bladder | Muscular layer of the wall of the urinary bladder. Synonym: tunica muscularis vesicae urinariae. (05 Mar 2000) |
| muscular coat of uterine tube | Muscular layer of the wall of the uterine tube. Synonym: tunica muscularis tubae uterinae. (05 Mar 2000) |
| muscular coat of uterus | <anatomy> Uterine smooth muscle. (18 Nov 1997) |
| muscular coat of vagina | Muscular layer of the vaginal wall. Synonym: tunica muscularis vaginae. (05 Mar 2000) |
| muscular dystrophy | A group of diseases characterised by progressive degeneration and/or loss of muscle fibres without nervous system involvement. All or nearly all of them have a hereditary origin but details of the type of genetic defect and of the prognosis for the disease vary from type to type. Duchenne muscular dystrophy (pseudohypertrophic muscular dystrophy) is the most common form. It is due to a sex-linked recessive allele and this is expressed as an absence of the protein dystrophin, the disease in boys shows extensive but insufficient muscle fibre reformation from satellite cells. (18 Nov 1997) |
| muscular fascia of extraocular muscle | Muscular fascia; the part of the orbital fascia that envelops the extraocular muscles; it is thin posteriorly but becomes thicker where it is continuous with the bulbar sheath; the fascial sheaths of the four rectus muscles are connected by an intermuscular membrane. Synonym: fascia muscularis musculorum bulbi, fascia of extraocular muscles, muscular fascia of extraocular muscle. (05 Mar 2000) |
| muscular fibril | <cell biology> Long cylindrical organelle of striated muscle, composed of regular arrays of thick and thin filaments and constituting the contractile apparatus. (18 Nov 1997) |
| muscular hyperesthesia | Sensitiveness of the muscles to pressure. (05 Mar 2000) |
| muscular incompetence | Imperfect closure of an anatomically normal cardiac valve, in consequence of defective action of its papillary muscles. (05 Mar 2000) |
| muscular insufficiency | Failure of any muscle to contract with its normal force, especially such failure of any of the eye muscles. (05 Mar 2000) |
| muscular lacuna | The lateral compartment beneath the inguinal (Poupart's) ligament, for the passage of the iliopsoas muscle and femoral nerve; it is separated by the iliopectineal arch from the vascular lacuna. Synonym: lacuna musculorum. (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) |
| Hoffmann's 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) |
| smooth muscular sphincter | A sphincter of smooth musculature. Synonym: smooth muscular sphincter. Origin: G. Lissos, smooth, + sphincter (05 Mar 2000) |
| spinal muscular atrophy | <radiology> 2nd most common autosomal recessive disease in Caucasians, pathology, degeneration of the spinal anterior horn cells, atrophy and wasting of skeletal muscles, types, SMA I = Werdnig-Hoffman disease: rapidly progressive, SMA II = intermediate form, SMA III = Kugelberg-Welander disease: slowly progressive, uncommon adult forms, usual presentations, floppy baby, arthrogryposis, muscle weakness in infancy, diagnosis, weakness and wasting with areflexia, electrophysiology shows anterior horm cell disease, genetics, linked to chromosome 5q., neuronal apoptosis inhibitory protein (NAIP) gene, survival motor neuron (SMN) gene (12 Dec 1998) |
| striated muscular sphincter | A sphincter made up of striated musculature. Synonym: striated muscular sphincter. Origin: rhabdo-+ G. Sphinkter, sphincter (05 Mar 2000) |
| Duchenne muscular dystrophy | A specific form of muscular dystrophy that is inherited as a sex-linked recessive trait and thus confined to young males and to females with Turner's syndrome. One third of all cases are estimated to be new mutational events. See: dystrophin. It is characterised by degeneration and necrosis of skeletal muscle fibres, that are replaced by fat and fibrous tissue. Symptoms include muscle weakness and in some forms, the appearance of muscle enlargement (pseudo-hypertrophy). Advanced cases can include weakness of the respiratory muscles (compromising breathing) and cardiomyopathy. Inheritance: sex-linked recessive. Incidence: 1 in 4000 male births. (11 Nov 1997) |
| idiopathic muscular atrophy | 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) |
| infantile 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) |
| infantile progressive 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) |
| 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) |
| 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) |
Synonyms : Limb-Girdle Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Muscular Dystrophy, Limb-Girdle, Limb Girdle Muscular Dystrophies, Limb Girdle Muscular Dystrophy, Muscular Dystrophies, Limb Girdle, Muscular Dystrophy, Limb Girdle
Synonyms : Animal Muscular Dystrophies, Animal Muscular Dystrophy, Dystrophies, Animal Muscular, Dystrophy, Animal Muscular, Muscular Dystrophies, Animal
Synonyms : Childhood Muscular Dystrophy, Pseudohypertrophic, Childhood Pseudohypertrophic Muscular Dystrophy, Duchenne-Type Progressive Muscular Dystrophy, Muscular Dystrophy, Childhood, Pseudohypertrophic, Muscular Dystrophy, Pseudohypertrophic, Childhood
Synonyms : Autosomal Dominant Emery-Dreifuss Muscular Dystrophy, Autosomal Recessive Emery-Dreifuss Muscular Dystrophy, Emery-Dreifuss Muscular Dystrophy 2, Emery-Dreifuss Muscular Dystrophy, Autosomal Recessive, Emery-Dreifuss Type Muscular Dystrophy
Synonyms : Facioscapulohumeral Atrophy, Facioscapulohumeral Type Progressive Muscular Dystrophy, Progressive Muscular Dystrophy, Facioscapulohumeral Type, Atrophies, Facioscapulohumeral, Atrophy, Facioscapulohumeral, Dystrophies, Facioscapulohumeral Muscular
| muscularity |
(mus
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
|---|---|
| muscularize |
(mus
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
| muscular rheumatism |
Fibromyalgia is a debilitating chronic syndrome (constellation of signs and symptoms) characterized by diffuse pain, fatigue, and a wide range of other symptoms. It is not contagious, and recent studies suggest that people with fibromyalgia may be genetically predispose. It affects more women than men, with a ratio globally of 3-5:1. Fibromyalgia is seen in 3-10% of the general population, and is mostly found between the ages 20 and 50. ...
출처: en.wikipedia.org/wiki/Muscular_rheumatism
|
| muscular system |
The muscular system is the biological system of animals that allows them to move internally and externally. The muscular system in vertebrates consists of three different types of muscles: cardiac, skeletal and smooth. Cardiac muscle is a striated muscle that makes up the heart. It is the only type of muscle consisting of branching fibers. Skeletal muscle consists of voluntary muscles attached to the frame of the skeletal system enabling bodily movement. ...
출처: en.wikipedia.org/wiki/Muscular_system
|
| muscular dystrophy |
An inherited disease that causes increasing weakness in muscle tissue; the muscles affected are the skeletal muscles and, occasionally, the muscles of the heart.
출처: highered.mcgraw-hill.com/sites/0072486694/student_...
|