| ¿µ¹® | myoclonus | ÇÑ±Û | °£´ë¼º±Ù°æ·Ã(Áõ) |
|---|---|---|---|
| ¼³¸í | ±ÙÀ°ÀÇ ÀϺÎ, ±ÙÀ° Àüü, ¶Ç´Â ÀϱºÀÇ ±ÙÀ°ÀÇ °©ÀÛ½º·¯¿î ¼öÃàÀ¸·Î¼ ½ÅüÀÇ ÀϺοµ¿ª¿¡ Á¦Çѵǰųª, ȤÀº ¿©·¯ ºÎÀ§¿¡¼ µ¿½Ã¼º ¶Ç´Â ºñµ¿½Ã¼ºÀ¸·Î ³ªÅ¸³´Ù. |
||
| ¿µ¹® | epilepsy | ÇÑ±Û | °£Áú |
|---|---|---|---|
| ¼³¸í | µ¹¹ßÀûÀ̰í ÀϰúÀûÀÎ ¹ßÀÛÀ» Ư¡À¸·Î ÇÏ´Â ¸¸¼º ÁßÃ߽Űæ°è ÁúȯÀÇ ÃÑĪÀÌ¸ç °øÅëÀûÀ¸·Î ¿îµ¿, Áö°¢, ÀÚÀ²½Å°æ°è ȤÀº Á¤½Å Áõ»óÀ» ³ªÅ¸³»°í °ÅÀÇ ¸ðµç °æ¿ì¿¡ ºñÁ¤»óÀûÀÎ ³úÆÄ ¾ç»óÀ» ³ªÅ¸³½´Ù. ³úÁ¶Á÷ÀÇ º´ÅÍ ¶Ç´Â ±â´ÉÀûÀÎ Àå¾Ö·Î ÀÎÇÏ¿© ¹ßÀÛÀûÀ¸·Î ½Å°æ±â´ÉÀå¾Ö¸¦ ÀÏÀ¸ÄÑ ¿©·¯ °¡Áö ½Å°æÁõ»ó, Áï µ¹¹ßÀûÀÎ ÀǽĻó½Ç, °æ·Ã, Á¤½Å ¶Ç´Â °¨°¢Àå¾Ö¸¦ ÀÏÀ¸Å°´Â Áúȯ, Àü°£ ¶Ç´Â Áö¶öº´À̶ó°íµµ ÇÑ´Ù. ÀüÀα¸ÀÇ ¾à 0.5%~1%¿¡¼ º¼ ¼ö ÀÖ´Â ÈçÇÑ Áúº´À¸·Î¼, Á¾Àü¿£ À¯Àüº´À̳ª ºÒÄ¡ÀÇ º´À¸·Î ´ÜÁ¤ÇÏ¿© Ä¡·á¸¦ ±âÇÇÇÏ´Â °æÇâÀÌ ÀÖ¾ú´Ù. ±×·¯³ª °£ÁúÀÇ ¿øÀΰú Ä¡·á¸é¿¡¼ ±Ù·¡¿¡ ¸¹Àº ¹ßÀüÀÌ ÀÖ¾î ÇöÀç´Â ¾à¹°Ä¡·á¿Í ³ú¼ö¼ú·Î½á °£Áú ȯÀÚÀÇ ¾à 80%¸¦ Ä¡À¯ÇÒ ¼ö ÀÖ´Ù. °£ÁúÀº ³úÀÇ ÀÌ»óÀ̳ª, ÀÌ¿¡ µû¸¥ Ư¡ÀûÀÎ ½ÅüÁõ»óµµ °°ÀÌ ³ªÅ¸³´Ù. ´Ù¾çÇÑ ÇüŰ¡ ÀÖÀ¸¸ç, ³úÆÄ°Ë»ç»ó Àü¹ÝÀûÀÎ ³úÀüüÀÇ ÀÌ»óÀÌ ³ªÅ¸³ª¸é Àü½Å¹ßÀÛ(generalized seizure(=epilepsy))À̶ó°í Çϸç, ÀϺÎÀÇ ³ú¿¡¼ ÀÌ»óÀÌ ³ªÅ¸³ª¸é ºÎºÐ¹ßÀÛ(partial seizure)À̶ó°í ÇÑ´Ù. ¶ÇÇÑ Àü½Å¹ßÀÛ¿¡´Â Å« ÆÈ´Ù¸®ÀÇ ¿îµ¿°ú ÀǽļҽÇ, ÀÚÀ²½Å°æÀÌ»ó µîÀ» È£¼ÒÇÏ´Â °¡Àå ½ÉÇÑ ÇüÅÂÀÇ ´ë¹ßÀÛ(grand mal seizure)¿Í, Àá±ñÀÇ ÀǽļҽǸ¸À» È£¼ÒÇÏ´Â ¼Ò¹ßÀÛ(petit mal seizure)°¡ ÀÖ´Ù. ±×¸®°í ºÎºÐ¹ßÀÛ¿¡´Â ¿îµ¿ºÎÀ§¿¡¸¸ ÀÌ»óÀÌ ³ªÅ¸³ª´Â ¿îµ¿¹ßÀÛ(motor seizure), °¨°¢ºÎÀ§¿¡¸¸ ÀÌ»óÀÌ ³ªÅ¸³ª´Â °¨°¢¹ßÀÛ(sensory seizure), ±×¸®°í °üÀÚ¿±ÀÇ ÀÌ»ó³úÆÄ¼Ò°ßÀ» ³ªÅ¸³»´Â °üÀÚ¿± ¹ßÀÛ(temporal lobe seizure) µîÀÌ ÀÖ´Ù. 3¼¼ ¼Ò¾Æ¿¡ ÀϾ°í, ´Ü¼øÈ÷ ÀǽļҽÇ(5~10Ãʰ£)À» ³ªÅ¸³½´Ù. |
||
| TLE | Temporal Lobe Epilepsy; ÃøµÎ¿± °£Áú = Psychomotor Epilepsy; Á¤½Å ¿îµ¿ °£Áú = Tem... |
|---|---|
| DME | degenerative myoclonus epilepsy; dimethyl diester; dimethyl ether; diphasic meningoencephalitis; dir... |
| JME | juvenile myoclonus epilepsy |
| MERRF | myoclonus epilepsy with ragged red fibers [syndrome] |
| MERRLA | myoclonus epilepsy-ragged red fibers-lactic acidosis [syndrome] |
| MERRF | Myoclonus epilepsy associated with ragged-red fibers |
|---|---|
| MERRF | Myoclonus epilepsy with ragged-red fibers |
| PME | Progressive Myoclonus Epilepsy |
| MERRF | myoclonus epilepsy and ragged red fiber |
| ADNFLE | Autosomal dominant nocturnal frontal lobe epilepsy |
| myoclonus epilepsy | A clinically diverse group of epilepsy syndromes, some benign, some progressive. Many are hereditary with mendelian and nonmendelian mitochondrial inheritance. All are characterised by the occurrence of myoclonus, which may be limited or predominate in the condition. Specific syndromes include cherry red spot myoclonus syndrome, ceroid lipofuscinosis, myoclonic epilepsy with ragged red fibres, and Baltic myoclonus. Synonym: localization related epilepsy. (05 Mar 2000) |
|---|
| Baltic myoclonus disease | One of the familial light sensitive myoclonic epilepsies. Unlike Lafora body polymyoclonus, where inclusion bodies are seen in the brain cells, the prognosis is often favourable. Probably an autosomal recessive disorder. (05 Mar 2000) |
|---|---|
| palatal myoclonus | Rhythmic contractions of the soft palate, the facial muscles, and the diaphragm, related to lesions of the olivocerebellar pathways. See: palatal nystagmus. (05 Mar 2000) |
| cherry-red spot myoclonus syndrome | <syndrome> A neuronal storage disorder in children characterised by a cherry red spot at the macula, progressive myoclonus, and easily controlled seizures; the result of sialidase deficiency. Type 1 is characterised by normal body habitus, cherry red macula, myoclonus, and normal beta-galactosidase levels; type 2 by short stature, bony abnormalities, and deficient beta-galactosidase. Synonym: sialidosis. (05 Mar 2000) |
| myoclonus | Twitching or spasm of a muscle or a group of muscles. (27 Sep 1997) |
| myoclonus multiplex | An ill-defined disorder marked by rapid and widespread muscle contractions. Synonym: paramyoclonus multiplex, polyclonia, polymyoclonus. (05 Mar 2000) |
| stimulus sensitive myoclonus | Myoclonus induced by a variety of stimuli, e.g., talking, calculation, loud noises, tapping, etc. (05 Mar 2000) |
| nocturnal myoclonus | Frequently repeated muscular jerks occurring at the moment of dropping off to sleep. (05 Mar 2000) |
| anosognosic epilepsy | Epilepsy characterised by attacks of which the person is unaware. Synonym: anosognosic seizures. (05 Mar 2000) |
| automatic epilepsy | <neurology> Seizures with elaborate and multiple sensory, motor, and/or psychic components. A common feature is the clouding of consciousness and amnesia for the event. Some clinical manifestations may include more complex behaviours like burst of anger, emotional outbursts, fear or automatisms. The EEG often reveals spike discharges in the temporal lobe during sleep. (02 Jan 1998) |
| autonomic epilepsy | Episodes of autonomic dysfunction presumably due to diencephalic irritation. Synonym: diencephalic epilepsy, vasomotor epilepsy, vasovagal epilepsy. (05 Mar 2000) |
| benign childhood epilepsy with centrotemporal spikes | A specific epilepsy syndrome beginning in childhood and remitting in adolescence, characterised by nocturnal simple partial motor seizures or generalised tonic-clonic seizures. EEG shows centrotemporal spikes that are activated by sleep and an otherwise normal EEG background. (05 Mar 2000) |
| major epilepsy | tonic-clonic seizure |
| vasomotor epilepsy | Episodes of autonomic dysfunction presumably due to diencephalic irritation. Synonym: diencephalic epilepsy, vasomotor epilepsy, vasovagal epilepsy. (05 Mar 2000) |
| vasovagal epilepsy | Episodes of autonomic dysfunction presumably due to diencephalic irritation. Synonym: diencephalic epilepsy, vasomotor epilepsy, vasovagal epilepsy. (05 Mar 2000) |
| generalised epilepsy | A major category of epilepsy syndromes characterised by one or more types of generalised seizures. (05 Mar 2000) |
| myoclonus epilepsy |
epilepsy characterized by clonus of muscle groups and progressive mental deterioration and genetic origin
Ãâó: wordnet.princeton.edu/perl/webwn
|
|---|
| myoclonus epilepsy | epilepsy characterized by clonus of muscle groups and progressive mental deterioration and genetic origin |
|---|
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¿© |
|---|