| MFS | Marfan syndrome; Medicare fee schedule |
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| MS | Maffuci syndrome; maladjustment score; mandibular series; Marfan syndrome; Marie-Strumpell [syndrome... |
| MFS | Marfan Syndrome |
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| MS | Marfan Syndrome |
| marfan syndrome | <radiology> Connective-tissue disorder: autosomal dominant, 15% sporadic, cardiovascular system (probable cause of death in 93%), aortic aneurysm (mostly ascending), dilatation of aortic sinuses, aortic dissection, coarctation, musculoskeletal system, tall stature, long limbs, arachnodactyly, lax joints, scoliosis (60%) / kyphosis / pectus, eye, lens subluxation Cf: homocystinuria More info: Marfan syndrome (12 Dec 1998) |
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| Marfan's disease | <syndrome> A hereditary condition of the connective tissue. Symptoms and signs include tall lean body type, irregular or unsteady gait, long extremities (including fingers and toes), abnormal joint flexibility, flat feet, stooped shoulders, dislocation of the optic lens and aneurysms of the aorta. Affects 1 in 50,000 people. Probably a collagen fibril assembly disorder since it can be mimicked in mice by aminonitriles that interfere with crosslinking. Inheritance: autosomal dominant. (06 Oct 1997) |
| Marfan's law | The healing of localised tuberculosis protects against subsequent development of pulmonary tuberculosis. (05 Mar 2000) |
| Marfan's syndrome | <syndrome> A hereditary condition of the connective tissue. Symptoms and signs include tall lean body type, irregular or unsteady gait, long extremities (including fingers and toes), abnormal joint flexibility, flat feet, stooped shoulders, dislocation of the optic lens and aneurysms of the aorta. Affects 1 in 50,000 people. Probably a collagen fibril assembly disorder since it can be mimicked in mice by aminonitriles that interfere with crosslinking. Inheritance: autosomal dominant. (06 Oct 1997) |
| Marfan, Antoine Bernard-Jean | <person> French paediatrician, 1858-1942. See: Marfan's disease, Marfan's law, Marfan's syndrome. (05 Mar 2000) |
| marfanoid | An obsolete term used of those whose phenotype bears a superficial resemblence to that of Marfan's syndrome. (05 Mar 2000) |
| syndrome, marfan | Inherited disorder with long fingers and toes, dislocation of the lens, and aortic wall weakness and aneurysm. (it has been suggested that abraham lincoln had marfan syndrome.) (12 Dec 1998) |
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Synonyms : Marfan's Syndrome, Arachnodactylies, Marfans Syndrome, Syndrome, Marfan, Syndrome, Marfan's
| Marfan syndrome |
An inheritable disorder of the connective tissue it affects the skeletal system, cardiovascular system, eyes, and skin. Iris coloboma can be one of the syndromes.
출처: www.geocities.com/coloboma_group/words.html
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| Marfan's sign |
a red triangle at the tip of a coated tongue indicates typhoid fever; a rarely observed phenomenon.
출처: www.merckmedicus.com/pp/us/hcp/thcp_dorlands_conte...
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| Marfan syndrome |
A condition that affects the connective tissue. Connective tissue holds the body together and provides support to many structures throughout the body. In Marfan syndrome, the body's connective tissue isn't normal. As a result, many body systems are affected, including the heart,blood vessels, bones, tendons, cartilage, eyes, nervous system, skin and lungs.
출처: www.clevelandclinic.org/heartcenter/pub/glossary/m...
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| Marfan syndrome |
Inherited disorder of the connective tissue, bones, muscles, ligaments, and skeletal structures. It is characterized by a tall lean body type with long extremities, abnormal joint flexibility, dislocation of the lens of the eye, cataracts, secondary glaucoma, myopia, strabismus, corneal flatness, and nystagmus.
출처: www.sparkle.usu.edu/glossary/syndromes_glossary.as...
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| Marfan syndrome |
an inherited disease affecting the bones, joints, heart and blood vessels.
출처: www.wvqualitycoalition.org/Media/VI.htm
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| Marfan | an autosomal dominant disease characterized by elongated bones (especially of limbs and digits) and abnormalities of the eyes and circulatory system |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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