| DMD | disease-modifying drug; Doctor of Dental Medicine; Duchenne muscular dystrophy; dystonia musculorum ... |
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| DM | defined medium; dermatomyositis; Descemet's membrane; dextromaltose; dextromethorphan; diabetes mell... |
| dy | dystrophia muscularis [mouse] |
| FOP | fibrodysplasia ossificans progressiva; forensic pathology |
| POP | diphosphate group; pain on palpation; paroxypropione; persistent occipitoposterior [fetal position];... |
| DM | Dystrophia myotonica |
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| FOP | Fibrodysplasia ossificans progressiva |
| poliodystrophia cerebri progressiva infantilis | Familial progressive spastic paresis of extremities with progressive mental deterioration, with development of seizures, blindness and deafness, beginning during the first year of life, and with destruction and disorganization of nerve cells of the cerebral cortex. Synonym: Alpers disease, Christensen-Krabbe disease, progressive cerebral poliodystrophy. (05 Mar 2000) |
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| myositis ossificans progressiva | <radiology> Progressive skeletal fusion, ossification of ligaments, nuchal ligament, pelvic entheses, asymptomatic at birth, 90% have short great toes (12 Dec 1998) |
| dysbasia lordotica progressiva | An affection characterised by lordoscoliosis of the lower portion of the vertebral column, occurring when the patient stands or walks and usually disappearing when the patient lies down. Synonym: torsion neurosis. (05 Mar 2000) |
| ophthalmoplegia progressiva | Progressive upper bulbar palsy, due to degeneration of the nuclei of the motor nerves of the eye. (05 Mar 2000) |
| leukodystrophia cerebri progressiva | <radiology> Type of dysmyelinating disease, hereditary, peripheral nervous system unaffected in some disorders Specific diseases: adrenoleukodystrophy, metachromatic leukodystrophy, spongy degeneration (Canavan), globoid cell (Krabbe) leukodystrophy, Alexander disease, Pelizaeus-Merzbacher disease, Cockayne syndrome (12 Dec 1998) |
| dystrophia | <pathology> Any disorder arising from defective or faulty nutrition, especially the muscular dystrophies. Origin: L. Dystrophia, Gr. Trephein = to nourish (18 Nov 1997) |
| dystrophia adiposogenitalis | A disorder characterised primarily by obesity and hypogonadotrophic hypogonadism in adolescent boys; dwarfism is rare, and when present is thought to reflect hypothyroidism. Visual loss, behavioural abnormalities, and diabetes insipidus may occur. Frohlich's syndrome often is used synonymously for this disorder, although the original case involved a pituitary tumour; most cases are thought to result from hypothalamic dysfunction in areas regulating appetite and gonadal development. The most common causes are pituitary and hypothalamic neoplasms. Synonym: adiposis orchica, adiposogenital degeneration, adiposogenital dystrophy, adiposogenital syndrome, hypophysial syndrome, hypothalamic obesity with hypogonadism. Origin: L. Fr. G. Dys-, bad, + trophe, nourishment (05 Mar 2000) |
| dystrophia brevicollis | A condition marked by symptoms of dystrophia adiposogenitalis together with a deforming shortness of the neck, but without synostosis of the cervical vertebrae seen in Klippel-Feil syndrome. (05 Mar 2000) |
| dystrophia myotonica | <neurology> An inherited human neuromuscular disease classed as an autosomal dominant disease in which there is progressive muscle weakening and wasting. A triplet repeat syndromes (like fragile X syndrome), this most common adult form of muscular dystrophy is caused by expansion of the unstable trinucleotide repeat CTG in the 3' untranslated region on chromosome 19q13 (cAMP-dependent muscle protein kinase gene). Anticipation has been associated with further expansion of the repeat upon transmission to subsequent generations (the inheritance pattern is autosomal dominant), although contraction has been noted to occur as well. Especially severe neonatal cases have been born to affected mothers preferentially, suggesting a role for genomic imprinting as well. The classic physical signs include atrophy of facial muscles, cataracts, and delayed muscle relaxation. Detection of the expanded trinucleotide repeat is accomplished by PCR or Southern blot and expansion appears to correlate with decreased transcription of the protein kinase gene. Inheritance: autosomal dominant. (29 Dec 1997) |
| dystrophia unguium | Dystrophy of the nails. (05 Mar 2000) |
| dystrophia ungulae | A condition of the hoof wall in the toe region of horses, characterised by loss of substance and change in character of the horn, most often as a sequela of mild chronic laminitis. Synonym: dystrophia ungulae, hollow wall. (05 Mar 2000) |
| bursa intermuscularis musculorum gluteorum | <anatomy> Two or three small bursae between the tendon of the gluteus maximus and the linea aspera. Synonym: bursa intermuscularis musculorum gluteorum, intermuscular gluteal bursa. (05 Mar 2000) |
| vagina communis musculorum flexorum | The synovial sheath that surrounds the eight tendons of the superficial and deep flexors of the digits of the hand as they pass through the carpal canal; it is commonly continuous with the digital sheath of the little finger. Synonym: vagina communis musculorum flexorum, ulnar bursa. (05 Mar 2000) |
| vagina tendinum musculorum abductoris longi et extensoris brevis pollicis | The synovial sheath lining the compartment of the extensor retinaculum that contains the abductor pollicis longus and extensor pollicis brevis tendons. Synonym: vagina tendinum musculorum abductoris longi et extensoris brevis pollicis. (05 Mar 2000) |
| vagina tendinum musculorum extensoris digitorum et extensoris indicis | The synovial sheath that surrounds the four tendons of the extensor digitorum muscle and the tendon of the extensor indicis deep to the extensor retinaculum. Synonym: vagina tendinum musculorum extensoris digitorum et extensoris indicis. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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