| ¿µ¹® | paralysis, palsy | ÇÑ±Û | ¸¶ºñ |
|---|---|---|---|
| ¼³¸í | ½Å°æÀ̳ª ±ÙÀ°ÀÌ ÇüÅÂÀÇ º¯È¾øÀÌ ±â´ÉÀ» ÀÒ¾î¹ö¸®´Â »óÅÂ. °¨°¢ÀÌ ¾ø¾îÁö°í, ¿òÁ÷ÀÏ ¼ö ¾ø´Â »óŸ¦ ¸»ÇÑ´Ù. ÀÌ·± ¸¶ºñ´Â ½Å°æ°èÀÌ»óÀÏ ¼öµµ ÀÖ°í, ÀüÇØÁú ÀÌ»óÀ¸·Î ÀÎÇÑ ÀÌ»óÀÏ ¼öµµ ÀÖÀ¸¸ç, ÇØ´ç ±ÙÀ°ÀÇ ¸¶ºñÀÏ ¼öµµ ÀÖ´Ù. ÀÌ·± °¢°¢ÀÇ °æ¿ì¿¡ ´ëÇØ ¸ðµÎ °¨º°Áø´ÜÀ» ÇØº¸¾Æ¾ß Çϸç, Ä¡·á ¶ÇÇÑ °¢°¢ ´Ù¸£´Ù. ¿îµ¿¸¶ºñ´Â ³ú¼Ó ¿îµ¿ÁßÃ߷κÎÅÍ ¸»ÃÊÀÇ ±ÙÀ°¼¶À¯ »çÀÌ¿¡ ¾î¶² Àå¾Ö°¡ Àֱ⠶§¹®¿¡ ÀϾ¸ç, ´Ü¸¶ºñ-¹Ý¸¶ºñ-´ë¸¶ºñ-»çÁö¸¶ºñ µîÀÌ ÀÖ´Ù. ´Ü¸¶ºñ´Â »ó-ÇÏÁö Áß 1Áö¸¸ÀÌ ¸¶ºñÇØ ÀÖ´Â °ÍÀ» ¸»Çϸç, ÁÖ·Î ´ë³ú°ÑÁú ¿îµ¿ºÎÀ§ Àå¾Ö ¶§¹®ÀÌ´Ù. ¹Ý¸¶ºñ´Â ½ÅüÀÇ ¾î´À ÇÑÂÊ ÁßÀÇ »ó-ÇÏÁö¿¡¼ º¼ ¼ö ÀÖÀ¸¸ç, ¸¶ºñ Áß¿¡¼µµ °¡Àå ¸¹°í, ¼Ó¼¶À¯¸· ºÎ±Ù¿¡ ³úÃâÇ÷-³úÇ÷ÀüÁõ-³ú»öÀüÁõ µîÀÇ Àå¾Ö°¡ ÀϾÀ» ¶§ ÀϾÙ. ´ë¸¶ºñ´Â ¾çÂÊ ÇÏÁö ¸¶ºñ¸¦ ¸»Çϸç, ô¼öÀå¾Ö·Î ÀÎÇÑ °æ¿ì°¡ ¸¹´Ù. »çÁö¸¶ºñ´Â ¾çÂÊÀÇ »ó-ÇÏÁö¿¡ ¸¶ºñ°¡ ¿Â °ÍÀ¸·Î¼ ¾çÂÊÀÇ ´ë³ú-ô¼ö-¸»ÃÊ½Å°æ µîÀÇ Àå¾Ö·Î ÀϾ¸ç, ¸ñô¼ö Àå¾Ö°¡ °¡Àå ¸¹´Ù. ÀÌ ¹Û¿¡µµ ¸»ÃʽŰ渶ºñ·Î ÀÎÇÑ ÀϺΠ±ÙÀ°¿îµ¿¸¶ºñµµ ÀÖ´Ù. ÀÓ»óÀûÀ¸·Î´Â ¾ó±¼½Å°æ¸¶ºñ-³ë»À½Å°æ¸¶ºñ-Á¤Á߽Ű渶ºñ-ÀÚ»À½Å°æ¸¶ºñ µîÀÌ ¾Ë·ÁÁ® ÀÖ´Ù. |
||
| DMD | Duchenne type Muscular Dystrophy; ¾Ç¼ºÇü DuchenneÇü ±ÙÀÌ¿µ¾çÁõ |
|---|---|
| PMD | Progressive Muscular Dystrophy; ÁøÇ༺ ±ÙÀÌ¿µ¾çÁõ Types of PMD(Progressive Muscular Dystroph... |
| DD | dangerous drug; data definition; day of delivery; degenerated disc; degenerative disease; delusional... |
| DMD | disease-modifying drug; Doctor of Dental Medicine; Duchenne muscular dystrophy; dystonia musculorum ... |
| AASP | acute atrophic spinal paralysis; American Association of Senior Physicians; ascending aorta synchron... |
| DMD | Duchenne type muscular dystrophy |
|---|---|
| AFP | Acute Flaccid Paralysis |
| HYPP | HYPERKALAEMIC periodic paralysis |
| HPP | Hyperkalemic periodic paralysis |
| HyperPP | Hyperkalemic periodic paralysis |
| Duchenne-Erb paralysis | A type of brachial birth palsy in which there is paralysis of the muscles of the upper arm and shoulder girdle (deltoid, biceps, brachialis, and brachioradialis muscles) due to a lesion of the upper trunk of the brachial plexus or of the roots of the fifth and sixth cervical roots. Synonym: Duchenne-Erb paralysis, Erb paralysis. (05 Mar 2000) |
|---|---|
| Aran-Duchenne disease | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
| Duchenne | Guillaume B.A., French neurologist, 1806-1875. See: Duchenne's disease, Duchenne's sign, Duchenne's syndrome, Duchenne-Aran disease, Aran-Duchenne disease, Duchenne-Erb paralysis, Duchenne dystrophy. (05 Mar 2000) |
| Duchenne-Aran disease | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
| Duchenne 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) |
| 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) |
| Duchenne's disease | 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) |
| Duchenne's sign | <clinical sign> Falling in of the epigastrium during inspiration in paralysis of the diaphragm. (05 Mar 2000) |
| Duchenne's syndrome | <syndrome> Subacute or chronic anterior spinal paralysis combined with multiple neuritis. (05 Mar 2000) |
| acute ascending paralysis | A paralysis of rapid course beginning in the legs and involving progressively the trunk, arms, and neck, ending sometimes in death in from one to three weeks. Synonym: ascending paralysis. (05 Mar 2000) |
| acute atrophic paralysis | Inflammation of the anterior cornua of the spinal cord; an acute infectious disease caused by the poliomyelitis virus and marked by fever, pains, and gastroenteric disturbances, followed by a flaccid paralysis of one or more muscular groups, and later by atrophy. Synonym: acute atrophic paralysis, myogenic paralysis. (05 Mar 2000) |
| ascending paralysis | A paralysis of rapid course beginning in the legs and involving progressively the trunk, arms, and neck, ending sometimes in death in from one to three weeks. Synonym: ascending paralysis. (05 Mar 2000) |
| ascending tick paralysis | <neurology> An ascending paralysis caused by the continued presence of Dermacentor and Ixodes ticks attached to the occipital or upper neck region in humans. The treatment consists of tick removal and supportive care. (27 Sep 1997) |
| Brown-Sequard's paralysis | <neurology, syndrome> A type of spinal cord lesion that is characterised by hemiparaplegia and hyperesthesia, but with loss of motor function on the same side as the lesion and hemianaesthesia on the opposite side. (27 Sep 1997) |
| bulbar paralysis | Progressive weakness and atrophy of the muscles of the tongue, lips, palate, pharynx, and larynx, usually occurring in later life; most often caused by motor neuron disease. Synonym: bulbar palsy, bulbar paralysis, Duchenne's disease, Erb disease, glossolabiolaryngeal paralysis, glossolabiopharyngeal paralysis. (05 Mar 2000) |
| Duchenne's paralysis |
Bulbar paralysis.
Ãâó:
|
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|