| mucoperiosteal | Relating to mucoperiosteum. (05 Mar 2000) |
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| mucoperiosteal flap | A flap composed of mucosa and periosteum, as from the hard palate or gingiva. (05 Mar 2000) |
| 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) |
| mucous cyst |
a retention cyst that contains mucus.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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| mucopolysaccharidosis |
The mucopolysaccharidoses are inborn errors of metabolism resulting from the deficiency of specific lysosomal enzymes needed in glycosaminoglycan catabolism. The glycosaminoglycans (GAGs) are complex carbohydrates that are major constituents of connective tissue. ...
출처: en.wikipedia.org/wiki/Mucopolysaccharidosis
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| mucosa |
The mucous membranes (or mucosae; singular: mucosa) are linings of ectodermic origin, covered in epithelium, and are involved in absorption and secretion. They line various body cavities that are exposed to the external environment and internal organs. It is at several places continuous with skin: at the nostrils, the lips, the ears, the genital area, and the anus. The sticky, thick fluid secreted by the mucous membranes and gland is termed mucus (note the spelling difference). ...
출처: en.wikipedia.org/wiki/Mucosa
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| mucous membrane |
The mucous membranes (or mucosae; singular: mucosa) are linings of ectodermic origin, covered in epithelium, and are involved in absorption and secretion. They line various body cavities that are exposed to the external environment and internal organs. It is at several places continuous with skin: at the nostrils, the lips, the ears, the genital area, and the anus. The sticky, thick fluid secreted by the mucous membranes and gland is termed mucus (note the spelling difference). ...
출처: en.wikipedia.org/wiki/Mucous_membrane
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| mucopurulent |
mixture of mucus and pus
출처: www.geocities.com/Heartland/Hollow/1991/medicat/me...
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