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  • hereditary disease
    À¯Àüº´
  • hereditary disorder
    À¯ÀüÀå¾Ö, À¯ÀüÁúȯ
  • hereditary epilepsy
    À¯Àü°£Áú
  • hereditary hearing impairment
    À¯Àüû·ÂÀå¾Ö
  • hereditary hemorrhagic telangiectasia
    À¯Àü¼ºÃâÇ÷¸ð¼¼Ç÷°üÈ®ÀåÁõ
  • hereditary leptocytosis
    À¯ÀüÇ¥ÀûÀûÇ÷±¸Áõ
  • hereditary lymphedema
    À¯Àü¸²ÇÁºÎÁ¾
  • hereditary methemoglobinemic cyanosis
    À¯Àü¸ÞÆ®Çì¸ð±Û·ÎºóÇ÷û»öÁõ
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´(Áõ)
  • hereditary multiple exostosis
    À¯Àü´Ù¹ß»Àµ¹ÃâÁõ, À¯Àü´Ù¹ß¿Ü°ñÁõ
  • hereditary mutilating keratoma
    À¯ÀüÀý´Ü°¢È­Á¾
  • hereditary nonpolyposis colorectal cancer
    1. À¯Àü¼ººñÆú¸³À߷ϰðâÀÚ¾Ï 2. À¯Àü¼ººñÆú¸³´ëÀå¾Ï
  • hereditary opalescent dentine
    À¯ÀüÁ¥ºû»ó¾ÆÁú
  • hereditary palmoplantar keratoderma
    À¯Àü¼Õ¹ß¹Ù´Ú°¢ÁúÇǺÎÁõ
  • hereditary spastic paraplegia
    À¯Àü°­Á÷ÇϹݽŸ¶ºñ
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    ÇѱÛ
  • hereditary coagulation disorder
    À¯ÀüÀÀ°íÀå¾Ö
  • hereditary opalescent dentine
    À¯ÀüÀ¯¹é»ö»ó¾ÆÁú
  • recessive hereditary disease
    ¿­¼ºÀ¯Àüº´
  • hereditary epilepsy
    À¯Àü°£Áú
  • hereditary bullous epidermolysis
    À¯Àü¹°ÁýÇ¥Çǹڸ®Áõ
  • hereditary multiple exostosis
    À¯Àü´Ù¹ß»Àµ¹ÃâÁõ
  • hereditary
    À¯Àü-
  • hereditary leptocytosis
    À¯ÀüÇ¥ÀûÀûÇ÷±¸Áõ
  • hereditary lymphedema
    À¯Àü¸²ÇÁºÎÁ¾
  • hereditary spherocytosis
    À¯ÀüµÕ±ÙÀûÇ÷±¸Áõ, À¯Àü±¸ÇüÀûÇ÷±¸Áõ
  • hereditary stigma
    À¯Àü¡ǥ
  • hereditary syphilis
    (¢¡congenital syphilis) ¼±Ãµ¸Åµ¶
  • hereditary trait
    À¯Àü¼ÒÁú
  • hereditary tremor
    (¢¡essential tremor) º»Å¶³¸², À¯Àü¶³¸², ¿øÀθ𸦶³¸²
  • hereditary adrenogenital syndrome
    À¯ÀüºÎ½Å¼º±âÁõÈıº
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
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    ÇѱÛ
  • pure red cell aplasia
    (ÁøÁ¤)ÀûÇ÷±¸°è ¹«Çü¼º(Áõ)(¡­Ùíû¡à÷ñø).
  • pure red cell aplasia
    (ÁøÁ¤)ÀûÇ÷±¸°è ¹«Çü¼º(Áõ)((òØïá)îåúìϹͧ Ùíû¡à÷ñø)
  • red cell aplasia
    ÀûÇ÷±¸¹«Çü¼º
  • red cell aplasia
    ÀûÇ÷±¸¹«Çü¼º(îåúìϹÙíû¡à÷)
  • renal aplasia
    ½Å¹«Çü¼º(Áõ)(ãìÙíû¡à÷ñø)
  • Hereditary camptodactyly
    À¯Àü¼º ±¼ÁöÁõ
  • hearing loss, congenital hereditary
    ¼±Ãµ(¼º) À¯Àü¼º ³­Ã»
  • hereditary
    À¯Àü¼ºÀÇ
  • hereditary adrenogenital syndrome
    À¯Àü¼º ºÎ½Å¼º±â¼º ÁõÈıº.
  • hereditary angioedema
    À¯Àü¼º ¸Æ°üºÎÁ¾
  • hereditary angioedema
    À¯Àü¼ºÇ÷°üºÎÁ¾
  • hereditary aphasia
    À¯Àü(¼º) ½Ç¾î(Áõ).
  • hereditary ataxia
    À¯Àü(¼º) ¿îµ¿½ÇÁ¶.
  • hereditary benign intraepithelial dyskeratosis
    À¯Àü¼º ¾ç¼º »óÇdz» ÀÌ»ó°¢È­Áõ
  • hereditary brown enamel
    À¯Àü¼º °¥»ö ¹ý³¶Áú.
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  • germinal aplasia
    ¹è¹«Çü¼ºÁõ(ÛÏÙíû¡à÷ñø).
  • germinal cell aplasia
  • gonadal aplasia
    ¼º¼±¹«Çü¼ºÁõ(¡­Ùíû¡à÷ñø).
  • megakaryocytic aplasia
    °ÅÇÙ±¸ Çü¼ººÎÀü(Áõ), °ÅÇÙ±¸¹«Çü¼º(Áõ)
  • nasal aplasia
    ºñ¹ßÀ°ºÎÀüÁõ
  • neocerebellar aplasia
    ½Å¼Ò³ú¹«Çü¼º.
  • pure red cell aplasia
    (ÁøÁ¤)ÀûÇ÷±¸°è ¹«Çü¼º(Áõ)(¡­Ùíû¡à÷ñø).
  • pure red cell aplasia
    (ÁøÁ¤)ÀûÇ÷±¸°è ¹«Çü¼º(Áõ)((òØïá)îåúìϹͧ Ùíû¡à÷ñø)
  • pure white cell aplasia
    (Áø¼º) ¹éÇ÷±¸°è¹«Çü¼º(Áõ)
  • red cell aplasia
    ÀûÇ÷±¸¹«Çü¼º
  • red cell aplasia
    ÀûÇ÷±¸¹«Çü¼º(îåúìϹÙíû¡à÷)
  • renal aplasia
    ½Å¹«Çü¼º(Áõ)(ãìÙíû¡à÷ñø)
  • transient red cell aplasia
  • uterine aplasia ³ª a. uteri
    Àڱù«Çü¼º(Áõ).
  • vaginal aplasia ³ª a. vaginalis
    Áú¹«Çü¼º(Áõ).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
CAPRCA chronic, acquired, pure red cell aplasia
CAVD complete atrioventricular dissociation; completion, arithmetic problems, vocabulary, following direc...
COACH cerebellar vermis hypoplasia/aplasia-oligophrenia-congenital ataxia-ocular colobomata-hepatic fibros...
CPRCA constitutional pure red cell aplasia
LPHAS limb/pelvis-hypoplasia/aplasia syndrome
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
BRB Blood Retinal Barrier
BREC bovine retinal endothelial cell
BRVO Branch retinal vein occlusion
CRA Central Retinal Artery
CRAO Central retinal artery occlusion
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  • ¿µ¹®
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    ¼³¸í
  • retinal
    ¸Á¸·ÀÇ
    1. ¸Á¸·¿¡ °üÇÑ. 2. ·¹Æ¼³îÀº ¾Ëµ¥ÇÏÀ̵å·Î¼­ À½½Ä¹°¿¡¼­ Èí¼öµÈ Ä«·ÎƾÀÌ »êÈ­ È¿¼Ò¿¡ ÀÇÇØ ºÐÇØµÇ¾î Çü¼ºµÇ¸ç, ºñŸ¹Î AÀÇ È°¼ºÀ» °¡Áø´Ù. ¸Á¸· ³»¿¡¼­ ·¹Æ¼³¯Àº ¿É½Å°ú °áÇÕÇÏ¿© °¨±¤ »ö¼Ò¸¦ Çü¼ºÇÑ´Ù. À̼ºÃ¼ÀÇ ÀÏÁ¾ÀÎ 11-cis retinalÀº °£»óü ÁßÀÇ ¿É½Å°ú °áÇÕÇÏ¿©, ·Îµ½½Å ¶Ç´Â ½ÃÈ«À» Çü¼ºÇÑ´Ù. ´Ù¸¥ À̼ºÃ¼ÀÎ 11- trans retinalÀº ·Îµ½½ÅÀÌ ºû¿¡ ÀÇÇÏ¿© Åð»öÇÏ¿© »ý±â¸ç, ¿©±â¿¡¼­ 11-cis ÇüÀÌ 11-trans ÇüÀ¸·Î ÀüȯµÈ´Ù. ·¹Æ¼³¯Àº ¿øÃßüÀÇ ¿É½Å°úµµ °áÇÕÇÏ¿© »ö°¢¿¡ °ü¿©ÇÏ´Â 3Á¾ÀÇ »ö¼Ò¸¦ Çü¼ºÇÑ´Ù.
  • retinal cell
    ¸Á¸· ¼¼Æ÷
  • retinal detachment
    ¸Á¸· ¹Ú¸®
  • retinal infiltrate
    ¸Á¸· ħÀ±
  • retinal neurocytoma
    ¸Á¸· ½Å°æ ¼¼Æ÷Á¾
  • retinal vasculopathy
    ¸Á¸· Ç÷°üº´Áõ
    1´Ü°è´Â ¼Òµ¿¸ÆÀÇ ÇùÂø, 2´Ü°è´Â µ¿Á¤¸Æ ÇÔ¿ä, ¼Ò·®ÀÇ »ïÃâ, ±×¸®°í ¼±»ó ÃâÇ÷¹Ý, 3´Ü°è´Â ¸Á¸· ºÎÁ¾, ÃâÇ÷, ±×¸®°í ¸éÈ­¹Ý, ½Å°æ ¼¶À¯Ãþ ³» ±¹¼Ò ÇãÇ÷, 4´Ü°è´Â 3´Ü°èÀÇ º¯È­¿Í ÇÔ²² À¯µÎ ºÎÁ¾ÀÌ´Ù.
  • retinal vein obstruction
    ¸Á¸· Á¤¸Æ Æó¼â
  • serous retinal detachment
    Àå¾×¼º ¸Á¸· ¹Ú¸®
  • hereditary
    À¯Àü¼º
    ºÎ¸ð·ÎºÎÅÍ ´ÙÀ½ ¼¼´ë·Î À¯ÀüÀÚ¿¡ ÀÇÇØ Àü´ÞµÇ´Â.
  • hereditary amyloidosis
    À¯Àü¼º À¯ÀüºÐÁõ
    1. À¯Àü¿¡ ÀÇÇØ ¿ø¼¶À¯¼º ´ç ´Ü¹éÀÌ ÇǺÎ, Á¡¸·, ³»ºÎ Àå±â¿¡ ħÀüµÇ´Â º´. 2. À¯ÀüÀûÀ¸·Î ½ÅüÀÇ °¢Á¾ ºÎÀ§¿¡ ¾Æ¹Ð·ÎÀ̵å
  • hereditary angioedema
    À¯Àü¼º ¸Æ°ü ºÎÁ¾, À¯Àü¼º Ç÷°ü ºÎÁ¾
    ½ÉºÎÀÇ ÁøÇÇ, ÇÇÇÏ Á¶Á÷, Á¡¸·ÇÏÁ¶Á÷À» ħ½ÀÇÏ´Â Ç÷°ü ¹ÝÀÀÀ¸·Î¼­, ¸ð¼¼Ç÷°üÀÇ È®Àå°ú Åõ°ú¼º Ç×Áø¿¡ ÀÇÇØ ÀϾ´Â ±¹ÇѼº ºÎÁ¾À» ³ªÅ¸³»¸ç °Å´ëÇÑ ÆØÁøÀÇ ¹ß»ýÀ» Ư¡À¸·Î ÇÑ´Ù. »ó¿°»öü¼º ¿ì¼º ÇüÁú·Î À¯ÀüÇÑ´Ù. »ê¹ß¼ºº¸´Ù ³»Àå º´º¯À» ´õ Àß ÀÏÀ¸Å°´Â °æÇâÀÌ ÀÖ´Ù.
  • hereditary aphasia
    À¯Àü ½Ç¾î, À¯Àü¼º ½Ç¾î, À¯Àü ½Ç¾îÁõ, À¯Àü¼º ½Ç¾îÁõ
  • hereditary brown tooth
    À¯Àü¼º °¥»ö Ä¡¾Æ
  • hereditary cerebrospinal paralysis
    ¿ìÀü¼º ³úô¼ö ¸¶ºñ
    º¸Åë Áß³â Ãʱ⿡ ÁøÇàÇÏ´Â À¯Àü¼º ÁúȯÀ¸·Î »óÁö ¶Ç´Â ÇÏÁöÀÇ ¾çÁö ¶Ç´Â ÀÏÃøÀ̳ª »çÁö¿¡ ³ªÅ¸³ª¸ç, ¼­¼­È÷ ÁøÇàµÇ´Â ¸¶ºñ°¡ Ư¡ÀÌ´Ù.
  • hereditary craniofacial dysostosis
    À¯Àü¼º µÎ°³ ¾È¸é À̰ñÁõ
    ž»ó µÎ°³, ¾È±¸ µ¹Ãâ, ¾ç¾È °Ý¸®, »ç½Ã, ¾Þ¹«»õ ºÎ¸® ¸ð¾ç1114-377786/377786Àüµ¹À» ¼ö¹ÝÇÏ´Â »ó¾Ç Çü¼º ºÎÀüÀ» Ư¡À¸·Î ÇÏ´Â À¯ÀüÀû Áúȯ.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
retinal 1. <anatomy> Pertaining to the retina.
2. <biochemistry> The aldehyde of retinol, derived by the oxidative enzymatic splitting of absorbed dietary carotene and having vitamin A activity. In the retina, retinal combines with opsins to form visual pigments. One isomer, 11 cis retinal combines with opsin in the rods (scotopsin) to form rhodopsin or visual purple. Another, all trans retinal (trans r.), visual yellow, xanthopsin) results from the bleaching of rhodopsin by light, in which the 11 cis form is converted to the all trans form. Retinal also combines with opsins in the cones (photopsins) to form the three pigments responsible for colour vision.
(18 Nov 1997)
retinal adaptation Adjustment to degree of illumination.
(05 Mar 2000)
retinal anlage tumour A benign neoplasm of neuroectodermal origin that most often involves the anterior maxilla of infants in the first year of life. It presents clinically as a rapidly growing blue-black lesion producing a destructive radiolucency; histologically, it is characterised by small round undifferentiated tumour cells interspersed with larger polyhedral melanin-producing cells arranged in an alveolar configuration.
Synonym: melanoameloblastoma, pigmented ameloblastoma, pigmented epulis, progonoma of jaw, retinal anlage tumour.
(05 Mar 2000)
retinal artery <anatomy, artery> Central retinal artery and its branches. It arises from the ophthalmic artery, pierces the optic nerve and runs through its centre, enters the eye through the porus opticus and branches to supply the retina.
(12 Dec 1998)
retinal artery occlusion Occlusion or closure of the central retinal artery causing sudden, usually nearly complete, loss of vision in one eye. Occlusion of the branch retinal artery causes sudden visual loss in only a portion of the visual field.
(12 Dec 1998)
retinal blood vessels The blood vasculature of the retina, including the branches and tributaries of the central retinal artery and vein, respectively, and the vascular circle of the optic nerve.
Synonym: vasa sanguinea retinae.
(05 Mar 2000)
retinal camera An instrument for photographing the ocular fundus.
(05 Mar 2000)
retinal cone <ophthalmology, physiology> One of the two photoreceptor cell types in the vertebrate retina.
In cones the photopigment is in invaginations of the cell membrane of the outer segment. Cones are less sensitive to light than rods, and are differentially sensitive to particular wavelengths of light and therefore important for colour vision.
They provide vision with higher spatial and temporal acuity, and it is the combination of signals from cones with different pigments that facilitates colour vision. There are three types of cones, each type sensitive to red, green or blue. Present in large numbers in the fovea.
(03 Jul 1999)
retinal degeneration <ophthalmology> A retrogressive pathological change in the retina, focal or generalised, caused by genetic defects, inflammation, trauma, vascular disease, or aging.
Degeneration affecting predominantly the macula lutea of the retina is macular degeneration.
(03 Jul 1999)
retinal dehydrogenase An oxidoreductase catalyzing the interconversion of retinaldehyde and NAD+ to retinoic acid and NADH; thus affecting growth and differentiation.
Synonym: retinaldehyde dehydrogenase.
(05 Mar 2000)
retinal detachment <ophthalmology> A painless disorder (when spontaneous) where the patient complains of a gradual raising or lowering of a curtain over the visual field of the affected eye. May also occur as the result of trauma.
(27 Sep 1997)
retinal disease <ophthalmology> A general term which describes any retinal changes (haemorrhages or exudates) that can affect vision (for example diabetic retinopathy, hypertensive retinopathy).
(27 Sep 1997)
retinal disparity The slight difference in retinal images that arises because of the lateral separation of the two eyes that stimulates stereoscopic vision.
(05 Mar 2000)
retinal drusen <ophthalmology> Colloid or hyaline bodies lying beneath the retinal pigment epithelium. They may occur either secondary to changes in the choroid that affect the pigment epithelium or as an autosomal dominant disorder of the retinal pigment epithelium.
(12 Dec 1998)
retinal dysplasia <ophthalmology> Congenital, often bilateral, retinal abnormality characterised by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary.
(12 Dec 1998)
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