| mucoperiosteum | Mucous membrane and periosteum so intimately united as to form practically a single membrane, as that covering the hard palate. (05 Mar 2000) |
|---|---|
| mucopolysaccharidase | <chemical> Mixture of an "eliminase" and a glucuronidase Chemical name: lyase, mucopolysaccharide Synonym: thiomucase (26 Jun 1999) |
| mucopolysaccharide | <biochemistry> The polysaccharide components of proteoglycans, now more usually known as glycosaminoglycans. (18 Nov 1997) |
| mucopolysaccharide keratin dystrophy | A histologic finding seen in the surface epithelium of oral inflammatory fibrous hyperplasia, consisting of homogeneous eosinophilic pools of material in the superficial spinous layer. (05 Mar 2000) |
| mucopolysaccharidoses | Inherited diseases in humans resulting from inability to break down glycosaminoglycans. Hunter syndrome and Hurler syndrome, for example: result from defects in lysosomal enzymes needed to break down sulphated mucopolysaccharides. (18 Nov 1997) |
| mucopolysaccharidosis | Any of a group of lysosomal storage diseases that have in common a disorder in metabolism of mucopolysaccharides, as evidenced by excretion of various mucopolysaccharides in urine and infiltration of these substances into connective tissue, with resulting various defects of bone, cartilage, and connective tissue. (05 Mar 2000) |
| mucopolysaccharidosis I | Systemic lysosomal storage disease caused by a deficiency of alpha-l-iduronidase and characterised by progressive physical deterioration with urinary excretion of dermatan sulfate and heparan sulfate. There are three recognised phenotypes representing a spectrum of clinical severity from severe to mild: hurler's syndrome, hurler-scheie syndrome and scheie's syndrome (formerly mucopolysaccharidosis v). Symptoms may include dwarfism, hepatosplenomegaly, gargoyle-like facies, corneal clouding, cardiac complications, and noisy breathing. (12 Dec 1998) |
| mucopolysaccharidosis II | Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of l-sulfoiduronate sulfatase. This disease differs from mucopolysaccharidosis I by slower progression, lack of corneal clouding, and x-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15. (12 Dec 1998) |
| mucopolysaccharidosis III | Mucopolysaccharidosis characterised by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme. (12 Dec 1998) |
| mucopolysaccharidosis IV | Genetic disorder of mucopolysaccharide metabolism characterised by skeletal abnormalities, joint instability, development of cervical myelopathy, and excessive urinary keratan sulfate. There are two biochemically distinct forms, each due to a deficiency of a different enzyme. (12 Dec 1998) |
| mucopolysaccharidosis vi | Mucopolysaccharidosis with excessive chondroitin sulfate b in urine, characterised by dwarfism and deafness. It is caused by a deficiency of n-acetylgalactosamine-4-sulfatase (arylsulfatase b). (12 Dec 1998) |
| mucopolysaccharidosis vii | Mucopolysaccharidosis characterised by excessive dermatan and heparan sulfates in the urine and hurler-like features. It is caused by a deficiency of beta-glucuronidase. (12 Dec 1998) |
| mucopolysacchariduria | The excretion of mucopolysaccharides in the urine. (05 Mar 2000) |
| mucoprotein | General term for a protein-polysaccharide complex, usually implying that the protein component is the major part of the complex, in contradistinction to mucopolysaccharide; mucoprotein's include the a1-and a2-globulins of serum (and others). Sometimes called glycoproteins, although this term usually refers to those mucoproteins's containing less than 4% carbohydrate. Tamm-Horsfall mucoprotein, the matrix of urinary casts derived from the secretion of renal tubular cells. (05 Mar 2000) |
| mucoproteins | Conjugated proteins in which mucopolysaccharides are combined with proteins. The mucopolysaccharide moiety is the predominant group with the protein making up only a small percentage of the total weight. (12 Dec 1998) |
Synonyms : Mucormycoses
Synonyms : Mucositides
Synonyms : Mucous Membranes, Membrane, Mucous, Membranes, Mucous, Mucosae, Muscularis, Mucosal Tissues, Propria, Lamina, Tissue, Mucosal, Tissues, Mucosal
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|---|---|---|---|
|
뮤코솔반고농축주사 - 새창
|
한국베링거인겔하임 |
Ambroxol HCl | 전문의약품 | 비급여 |
|
|
뮤코후르드나잘스프레이 - 새창
|
UCB |
E05920021 | Mesna | 일반의약품 | 삭제 |
|
무코치올정 - 새창
|
삼일제약 |
A05002951 | Methyl N,S diacetylcysteinate, Protease | 일반의약품 | 비급여 |
|
뮤코리드캅셀200mg - 새창
|
제이알피 |
A09050431 | Acetylcysteine | 일반의약품 | 급여 |
|
뮤코렉스캅셀 - 새창
|
경인제약 |
A29400241 | Sobrerol | 일반의약품 | 비급여 |
|
무코신일정 - 새창
|
신일제약 |
A20704811 | Methyl N,S diacetylcysteinate | 일반의약품 | 급여 |
|
무코신일산 - 새창
|
신일제약 |
A20704821 | Methyl N,S diacetylcysteinate | 일반의약품 | 급여 |
|
뮤코세린캅셀 - 새창
|
한국휴텍스제약 |
A00850231 | Acetylcysteine | 일반의약품 | 급여 |
|
뮤코브이시럽 - 새창
|
이연제약 |
A01450761 | Ambroxol HCl | 일반의약품 | 급여 |
|
뮤코브이정 - 새창
|
이연제약 |
A01450701 | Ambroxol HCl | 일반의약품 | 급여 |
| mucosal |
of or relating to mucous membranes
출처: wordnet.princeton.edu/perl/webwn
|
|---|---|
| mucoid colony |
one that is large, dome-shaped, and shiny, containing large quantities of capsular polysaccharide material that may be drawn out in viscous strings by a needle; called also M c.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
| mucocutaneous junction |
the site of transition between skin and mucous membrane.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
| mucogingival junction |
a sharply scalloped, generally indistinct line running parallel with the free margin, separating the gingival tissue from that of the oral mucosa; visible under the microscope. Called also mucogingival line.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
| mucoperiosteal flap |
a flap of mucosal tissue, including the periosteum, reflected from bone.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
