| ¿µ¹® | deafness | ÇÑ±Û | ±Í¸ÔÀ½, ³Ã» |
|---|---|---|---|
| ¼³¸í | û°¢ÀÌ ÀúÇÏ ¶Ç´Â »ó½ÇµÈ »óÅÂ. ¿øÀΰú Á¤µµ´Â ¿©·¯ °¡ÁöÀε¥, ±Í¸Ó°Å¸®´Â ±× Á¤µµ°¡ °¡Àå ½ÉÇÑ »óÅÂÀÌ´Ù. û°¢ÀÇ Àüµµ°æ·Î¿¡ Àå¾Ö°¡ ÀÖÀ» ¶§ ³Ã»ÀÌ ÀϾ°í, ±× º´ÅͰ¡ ¹Ù±ù±Í±æÀ̳ª °¡¿îµ¥±Í¿¡ ÀÖ´Â °ÍÀ» ÀüÀ½³Ã», ¼Ó±Í¿¡ ÀÖ´Â °ÍÀ» °¨À½³Ã»À̶ó ÇÏ¿© ±¸ºÐÇÑ´Ù. ¶Ç º´ÅÍÀÇ ÀÚ¸®¸¦ ¸í½ÃÇÏ¿© ÁßÀ̼º ³Ã»À̳ª ¹Ì·Î¼º ³Ã» µîÀ¸·Î ¼¼ºÐÇϱ⵵ Çϸç, ¿Ü»ó¼º ³Ã» µî ¿øÀκ°·Î ºÐ·ùÇϱ⵵ ÇÑ´Ù. ³Ã»ÀÇ Áø´ÜÀ̳ª ¿¹¹æ-¿¹ÈĴ û·Â°Ë»ç¿¡ ÀÇÇÏ¿© ½Ç½ÃµÈ´Ù. |
||
| ¿µ¹® | albinism | ÇÑ±Û | ¹éÇÇÁõ, ¹é»öÁõ |
|---|---|---|---|
| ¼³¸í | ¼±Ãµ¼ºÀ¸·Î ¸á¶ó´Ñ(ÇǺÎ, ¸ð¹ß, ´«ÀÇ »öÀ» ³ªÅ¸³»´Â Àΰ£ÀÇ »ö¼Ò)ÀÇ °áÇÌÀ¸·Î ÀÎÇÏ¿© ¸ð¹ß, ÇǺΠȤÀº ´«¿¡ »ö°¥ÀÌ ¾ø¾î Èñ°Ô º¸ÀÌ°Ô µÇ´Â º´. ¸á¶ó´ÑÀº Àڿܼ±À» Èí¼öÇÏ¿© ÇǺθ¦ Å¾籤¼±À¸·Î ºÎÅÍ º¸È£ÇÏ´Â ÀÛ¿ëÀÌ Àֱ⠶§¹®¿¡ ÀÌ º´°ú °°ÀÌ ¸á¶ó´ÑÀÌ ¾øÀ» °æ¿ì¿¡ ÅÂ¾ç ±¤¼±¿¡ ÀÇÇÑ ÇǺÎÀÇ ¼Õ»óÀÌ ½ÉÇØÁö°í ÇǺξϰú ±âŸÀÇ ¾ÏÀÇ À§ÇèÀÌ ³ô´Ù. |
||
| ADFN | albinism-deafness [syndrome]; albinism-deafness syndrome |
|---|---|
| OASD | ocular albinism-sensorineural deafness [syndrome] |
| ALDS | albinism-deafness syndrome |
| BADS | black locks-albinism-deafness syndrome |
| AROA | autosomal recessive ocular albinism |
| OA1 | Ocular albinism type 1 |
|---|---|
| SNHL | Sensorineural Hearing Loss |
| MIDD | Maternally Inherited Diabetes and Deafness |
| OCA | Oculocutaneous albinism |
| SD | Sudden deafness |
| sensorineural deafness | Hearing impairment due to disorders of the cochlear division of the 9th cranial nerve (auditory nerve), the cochlea, or the retrocochlear nerve tracts, as opposed to conductive deafness. (05 Mar 2000) |
|---|---|
| albinism, ocular | Albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. The classic type is x-linked (nettleship-falls), but an autosomal recessive form also exists. Ocular abnormalities may include reduced pigmentation of the iris, nystagmus, photophobia, strabismus, and decreased visual acuity. (12 Dec 1998) |
| ocular albinism | The absence of pigment chiefly in the iris, choroid, and retinal pigment epithelium with deafness; X-linked inheritance. (05 Mar 2000) |
| hearing loss, sensorineural | Hearing loss resulting from damage to the sensory mechanism internal from the oval and round windows. (12 Dec 1998) |
| sensorineural hearing loss | <neurology> A form of deafness that occurs due to dysfunction of the auditory nerve (cranial nerve VIII). (27 Sep 1997) |
| albinism | <dermatology> Condition in which no melanin (or other pigment) is present. (05 Feb 1998) |
| albinism, oculocutaneous | Heterogeneous group of autosomal recessive disorders comprising at least four recognised types, all having in common varying degrees of hypopigmentation of the skin, hair, and eyes. The two most common are the tyrosinase-positive and tyrosinase-negative types. (12 Dec 1998) |
| rufous albinism | A pigmentary anomaly of blacks, characterised by red or yellow-red hair colour, copper-red skin, and often by dilution of iris pigment. Synonym: rufous albinism. Origin: G. Xanthos, yellowish (05 Mar 2000) |
| cutaneous albinism | An autosomal dominant condition characterised by patterned loss of skin pigment on extremities and ventral thorax; a white forelock is often present, but no ocular findings. (05 Mar 2000) |
| oculocutaneous albinism | An autosomal recessive deficiency of pigment in skin, hair, and eyes; in the tyrosinase negative type, there is an absence of tyrosinase; in the tyrosinase positive type, there is normal tyrosinase which cannot enter pigment cells; it is transmitted by an autosomal recessive inheritance. The compound heterozygote is normal so the two forms are not allelic. There are several types: type IA is characterised by absence of tyrosinase with life-long complete absence of melanin, marked photophobia, and nystagmus. Type IB, yellow albinism with low or absent tyrosinase; improves with age. Type II, with normal tyrosinase activity is the most common; hair darkens and nevi and freckles develop. Type III is characterised by absent tyrosinase but pigmentation of the iris in the first decade. Type IV in Africans with normal tyrosinase. Type V with red hair. Type VI, Hermansky-Padlak syndrome, with haemorrhage due to platelet deficiency and low to absent tyrosinase. Synonym: Hermansky-Pudlak syndrome type VI. (05 Mar 2000) |
| acoustic trauma deafness | Sensorineural hearing loss due to overexposure to high intensity noise levels. Synonym: boilermaker's deafness, industrial deafness, occupational deafness. (05 Mar 2000) |
| Alexander's deafness | High frequency deafness due to membranous cochlear dysplasia. (05 Mar 2000) |
| boilermaker's deafness | Sensorineural hearing loss due to overexposure to high intensity noise levels. Synonym: boilermaker's deafness, industrial deafness, occupational deafness. (05 Mar 2000) |
| central deafness | Deafness due to disorder of the auditory system of the brainstem or cerebral cortex. (05 Mar 2000) |
| retrocochlear deafness | Former term for sensorineural deafness; suggesting a lesion proximal to the cochlea. (05 Mar 2000) |
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