| 영문 | albinism | 한글 | 백피증, 백색증 |
|---|---|---|---|
| 설명 | 선천성으로 멜라닌(피부, 모발, 눈의 색을 나타내는 인간의 색소)의 결핍으로 인하여 모발, 피부 혹은 눈에 색갈이 없어 희게 보이게 되는 병. 멜라닌은 자외선을 흡수하여 피부를 태양광선으로 부터 보호하는 작용이 있기 때문에 이 병과 같이 멜라닌이 없을 경우에 태양 광선에 의한 피부의 손상이 심해지고 피부암과 기타의 암의 위험이 높다. |
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| ADFN | albinism-deafness [syndrome]; albinism-deafness syndrome |
|---|---|
| HCG, hCG | Human Chorionic Gonadotropin; 사람융모성성선자극호르몬 1. Placental Glycoprotein Hormone &nbs... |
| AR | 1) Aortic Regurgitation = AI Echo소견 &... |
| OCA | Oculo-Cutaneous Albinism |
| ALDS | albinism-deafness syndrome |
| OA1 | Ocular albinism type 1 |
|---|---|
| OCA | Oculocutaneous albinism |
| ACC | Agenesis of the corpus callosum |
| CC | Corpus callosum |
| CL | Corpus luteum |
| albinism | <dermatology> Condition in which no melanin (or other pigment) is present. (05 Feb 1998) |
|---|---|
| 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) |
| 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) |
| ocular albinism | The absence of pigment chiefly in the iris, choroid, and retinal pigment epithelium with deafness; X-linked inheritance. (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) |
| agenesis of corpus callosum | <radiology> Defect in dorsal portion of lamina reuniens, occurs about 10th - 12th week of gestation, may be complete or partial CT findings: parallel lateral ventricles, occipital horns dilated, deep falx, frontal horns C-shaped on coronal view associated with, Dandy-Walker cyst, encephalocele, Arnold-Chiari malformation, CNS lipoma (12 Dec 1998) |
| atretic corpus luteum | A retrogressed corpus luteum characterised by increasing cicatrization and shrinkage of the cicatricial core with an amorphous, convoluted, completely hyalinised lutein zone surrounding the central plug of scar tissue. Synonym: albicans, atretic corpus luteum, corpus candicans. Corpora allata, a pair of juvenile hormone-producing endocrine glands located near the brain in insects; action of the juvenile hormone is interrelated with that of brain hormone and ecdysone; a high concentration of the hormone at the time of molting will cause production of an additional larval instar; removal at an early larval stage causes precocious pupation, resulting in the formation of a midget adult; implantation at late larval stages can cause development of an oversized adult. (05 Mar 2000) |
| bulb of corpus spongiosum | The expanded posterior part of the corpus spongiosum of the penis lying in the interval between the crura of the penis. Synonym: bulbus penis, bulb of corpus spongiosum, bulb of urethra, bulbus urethrae. (05 Mar 2000) |
| radiation of corpus callosum | The spreading out of the fibres of the corpus callosum in the centrum semiovale of each cerebral hemisphere. Synonym: radiatio corporis callosi. (05 Mar 2000) |
| vein of corpus striatum | <anatomy, vein> A long vein passing forward in the groove between the thalamus and caudate nucleus, covered by the lamina affixa, receiving the transverse caudate veins along its lateral side, and joining at the caudal wall of Monro's foramen with the choroidal vein and vein of septum pellucidum to form the internal cerebral vein. Synonym: vena terminalis, vena thalamostriata superior, terminal vein, vein of corpus striatum. (05 Mar 2000) |
| genu of corpus callosum | The anterior extremity of the corpus callosum that folds downward and backward on itself, terminating in the rostrum. Synonym: genu corporis callosi. (05 Mar 2000) |
| parenchymatous cell of corpus pineale | A cell of the pineal body with long processes ending in bulbous expansions. Pinealocytes receive a direct innervation from sympathetic neurons that form recognizable synapses. The club-shaped endings of pinealocyte processes terminate in perivascular spaces surrounding capillaries. Synonym: chief cell of corpus pineale, parenchymatous cell of corpus pineale. Origin: pineal + G. Kytos, cell (05 Mar 2000) |
| caverns of corpus spongiosum | The vascular spaces forming the erectile tissue of the corpus spongiosum penis in the male and the bulb of the vestibule in the female. Synonym: cavernae corporis spongiosi, cavities of corpus spongiosum. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|