| ¿µ¹® | neurofibromatosis | ÇÑ±Û | ½Å°æ¼¶À¯Á¾Áõ |
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| ¼³¸í | Àü½ÅÀÇ ¿©·¯°÷¿¡ ¹«´õ±â·Î ³ª´Â ½Å°æ¼¶À¯Á¾À» Ư¡À¸·Î ÇÏ´Â À¯Àü¼º Àü½Å º´. ¸»ÃÊ ½Å°æ»Ó ¾Æ´Ï¶ó ÁßÃß ½Å°æ°èµµ ħ¹üÇÒ ¼ö ÀÖ´Ù. ½Å°æ¼¶À¯Á¾Àº ÁÖ·Î Àü½ÅÀÇ ÇǺο¡ ¹ß»ýµÇÁö¸¸ ½Å°æ¾ó±â ȤÀº ³»Àå¿¡ »ý±â´Â ¼öµµ ÀÖ´Ù. ÇǺο¡´Â ¶ÇÇÑ °÷°÷¿¡ ƯÀ¯ÀÇ °¥»ö»ö¼Ò¹ÝÀ» º¸°Ô µÈ´Ù. °ñ°ÝÀÇ º¯ÇüÀ» ÀÏÀ¸Å³ ¼öµµ ÀÖ´Ù. ½Å°æÃÊÁ¾À̳ª ¾Ç¼º½Å°æÃÊÁ¾, ´õ¿íÀÌ ½Å°æ±³Á¾À̳ª ¼ö¸·Á¾ µîÀÇ µÎ°³³»Á¾¾çÀ» ÇÕº´ÇÔµµ ¾Ë·ÁÁ® ÀÖ´Ù. 1Çü(von Recklinghausen º´, ÀüÇüÀû ½Å°æ¼¶À¯Á¾Áõ)°ú 2Çü(ÁßÃßÇü ¶Ç´Â û°¢½Å°æ¼¶À¯Á¾Áõ)À¸·Î ±¸ºÐÇÑ´Ù. ÀüÇüÀû ½Å°æ¼¶À¯Á¾Áõ(1Çü)ÀÌ °¡Àå ¸¹ÀÌ ¹ß»ýÇÏ¸ç ´ÙÀ½°ú °°Àº 3°¡Áö ¼Ò°ßÀ» º¸Àδô. Áï ¨ç üǥ¸é, ü³» ¿©·¯ °÷¿¡ »êÀçµÇ¾î ¹ß»ýÇÏ´Â ¾ó±â¸ð¾ç½Å°æÁ¾, ¨è ¿ìÀ¯Ä¿ÇǹÝÁ¡, ¨é ¸®½¬(Lisch) °áÀý·Î ºÒ¸®´Â ȫäÀÇ Âø»ö°ú¿ÀÁ¾ÀÌ´Ù. 2ÇüÀº 1Çüº¸´Ù ¹ß»ýºóµµ°¡ Àû°í, Ư¡ÀûÀ¸·Î ¾çÂʼº û°¢½Å°æÁ¾ÀÌ ÀÖÀ¸¸ç, ¿ìÀ¯¹ÝÁ¡Àº º¸À̳ª ¸®½¬°áÀýÀº ¾ø´Ù. |
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| ¿µ¹® | central nervous system(CNS) | ÇÑ±Û | ÁßÃ߽Űæ°è |
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| ¼³¸í | ½Å°æ°è´Â ÁßÃ߽Űæ°è¿Í ¸»ÃʽŰæ°è·Î ºÐ·ùÇÒ ¼ö°¡ ÀÖ´Ù. ÁßÃ߽Űæ°è¶õ ³ú¿Í ô¼ö·Î ±¸¼ºµÇ¾î ÀÖ´Â ½Å°æ°è¸¦ À̸£´Â ¸»ÀÌ´Ù. ¸»ÃʽŰæ°è¶õ ÀÌ ÀÌ¿ÜÀÇ ¸ðµç ½Å°æ°è¸¦ À̸£´Â ¸»ÀÌ´Ù. |
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| NF | nafcillin; National Formulary; nephritic factor; neurofibromatosis; neurofilament; neutral fraction;... |
|---|---|
| NF1 | neurofibromatosis type I; nuclear factor 1 |
| NF2 | neurofibromatosis type II |
| NFNS | neurofibromatosis-Noonan syndrome |
| NPDC | neurofibromatosis-pheochromocytoma-duodenal carcinoid [syndrome] |
| NF1 | NEUROFIBROMATOSIS TYPE 1 |
|---|---|
| NF | Neurofibromatosis |
| NF 1 | Neurofibromatosis |
| NF 1 | Neurofibromatosis 1 |
| NF 2 | Neurofibromatosis 2 |
| central type neurofibromatosis | Type I neurofibromatosis. Incomplete neurofibromatosis, multiple neurofibromas with minimal manifestations, perhaps limited to cafe-au-lait spots; individuals with minimal lesions may have offspring with severe involvement. Synonym: abortive neurofibromatosis. (05 Mar 2000) |
|---|---|
| abortive neurofibromatosis | incomplete neurofibromatosis |
| genes, neurofibromatosis 1 | Tumour suppressor genes located on the long arm of human chromosome 17 in the region 17q11.2. Mutation of these genes is thought to cause neurofibromatosis 1. (12 Dec 1998) |
| genes, neurofibromatosis 2 | Tumour suppressor genes located on the long arm of human chromosome 22. Mutation or loss of these genes causes neurofibromatosis 2. (12 Dec 1998) |
| neurofibromatosis | <oncology> One of the most common disorders in genetics, neurofibromatosis encompasses at least two diseases, designated NF-1 and NF-2. NF-1 or classic neurofibromatosis, is characterised by the familiar cafe- au-lait spots, axillary freckling, cutaneous and visceral neurofibromas (which sometimes undergo malignant transformation), gliomas, scoliosis, and Lisch nodules of the iris. NF-1 is associated with the the von Recklinghausen Neurofibromatosis locus that encodes the NF-1 protein, a GTPase activating protein which interacts with the ras proteins. The gene is located on chromosome 17. NF-2, also called acoustic or central neurofibromatosis, features neurofibromas restricted to the acoustic nerve (usually bilateral) and the central nervous system, skin lesions may or may not be present. The gene is located on chromosome 22. There are no biochemical markers of the disorder, but the cloning of both the NF-1 and NF-2 genes makes DNA-based diagnosis possible in some families. Both genes appear to be tumour suppressor genes. Both conditions are autosomal dominant, but the variable penetrance and expressivity and high frequency of new mutations make genetic counseling difficult. Inheritance: autosomal dominant. (29 Dec 1997) |
| neurofibromatosis 1 | A congenital autosomal dominant disorder characterised by developmental changes in the nervous system, muscles, bones, and skin especially in those derived from the embryonic neural crest. There are multiple cutaneous tumours and tumours of the peripheral and central nervous system. The disease has been linked to mutations of the nf1 gene on chromosome 17. (12 Dec 1998) |
| neurofibromatosis 2 | Severe autosomal dominant disorder characterised especially by bilateral acoustic neuromas as well as other multiple tumours including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the nf2 gene on chromosome 22. (12 Dec 1998) |
| ala central lobule | The lateral winglike projection of the central lobule of the cerebellum. Synonym: ala lobuli centralis, ala cerebelli. (05 Mar 2000) |
| anterior central convolution | Bounded posteriorly by the central sulcus and anteriorly by the precentral sulcus. Synonym: gyrus precentralis, anterior central convolution, anterior central gyrus, ascending frontal convolution, ascending frontal gyrus. (05 Mar 2000) |
| anterior central gyrus | Bounded posteriorly by the central sulcus and anteriorly by the precentral sulcus. Synonym: gyrus precentralis, anterior central convolution, anterior central gyrus, ascending frontal convolution, ascending frontal gyrus. (05 Mar 2000) |
| anterolateral central arteries | Numerous small branches from the sphenoidal part of the middle cerebral arteries supplying the lateral and anterior parts of the corpus striatum. Synonym: arteriae centrales anterolaterales, arteriae thalamostriatae anterolaterales, anterolateral central arteries, anterolateral striate arteries, anterolateral thalamostriate arteries, arteries of cerebral haemorrhage, lenticulostriate arteries. (05 Mar 2000) |
| anteromedial central arteries | Several small branches of the precommunical part of the anterior cerebral artery; they are distributed to the anteromedial part of the corpus striatum part of the thalamus. Synonym: arteriae centrales anteromediales, arteriae thalamostriatae anteromediales, anteromedial thalamostriate arteries. (05 Mar 2000) |
| anteromedial central branches | Branches of the anterior communicating artery which supply part of the hypothalamus. Synonym: rami centrales anteromediales. (05 Mar 2000) |
| artery of central sulcus | <anatomy, artery> A branch of the terminal part of the middle cerebral artery distributed to the cortex on either side of the central sulcus. Synonym: arteria sulci centralis, artery of central sulcus, central artery, Rolandic artery. (05 Mar 2000) |
| asia, central | The geographical area of asia comprising kazakhstan, kyrgyzstan, tajikistan, turkmenistan, and uzbekistan. The desert region of kara kum (qara qum) is largely in turkmenistan and the desert region of kyzyl kum (kizil kum or qizil qum), is in uzbekistan and kazakhstan. (12 Dec 1998) |
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