| ¿µ¹® | albinism | ÇÑ±Û | ¹éÇÇÁõ, ¹é»öÁõ |
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| ADFN | albinism-deafness [syndrome]; albinism-deafness syndrome |
|---|---|
| OCA | Oculo-Cutaneous Albinism |
| AR | 1) Aortic Regurgitation = AI Echo¼Ò°ß &... |
| ALDS | albinism-deafness syndrome |
| AROA | autosomal recessive ocular albinism |
| OA1 | Ocular albinism type 1 |
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| OCA | Oculocutaneous albinism |
| ACA | Active cutaneous anaphylaxis |
| ACL | American Cutaneous Leishmaniasis |
| CFC | Cardio-Facio-Cutaneous |
| 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) |
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| albinism | <dermatology> Condition in which no melanin (or other pigment) is present. (05 Feb 1998) |
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| 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) |
| 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) |
| acute cutaneous leishmaniasis | A form of cutaneous leishmaniasis characterised by rural distribution of human cases near infected rodents, particularly communal ground squirrels; characterised by acute rapidly developing dermal lesions that become severely inflamed, with moist necrotizing sores or ulcers that heal in two to eight months after a two to four month incubation period; among nonimmune immigrants, multiple lesions may develop, which heal more slowly and leave disabling or disfiguring scars. A strong delayed hypersensitivity and involvement of immune complexes play a role in necrosis, which is part of the healing process and of the strong specific immunity that follows. Synonym: acute cutaneous leishmaniasis, rural cutaneous leishmaniasis, wet cutaneous leishmaniasis. (05 Mar 2000) |
| administration, cutaneous | The application of suitable drug dosage forms to the skin for either local or systemic effects. (12 Dec 1998) |
| anterior cutaneous branches of intercostal nerves | Medial mammary branches of anterior cutaneous branches of ventral primary rami of thoracic spinal nerves. See: medial mammary branches. (05 Mar 2000) |
| anterior cutaneous branch of iliohypogastric nerve | <anatomy, nerve> Distribution, skin on pubis. Synonym: ramus cutaneus anterior nervi iliohypogastrici, genital branch of iliohypogastric nerve. (05 Mar 2000) |
| anterior cutaneous nerves of abdomen | The ventral primary rami of spinal nerves T7-T11 (seventh to eleventh intercostal nerves), which supply the abdominal as well as the thoracic wall; innervate intercostal, subcostal, serratus posterior inferior, transversus abdominis, external and internal oblique, and rectus abdominis muscles, and provide sensory branches to the periphery of the diaphragm, and parietal pleura and peritoneum. Synonym: rami cutanei anteriores pectoralis et abdominalis nervorum intercostalium, ramus cutaneus anterior (pectoralis et abdominalis) nervorum thoracicorum, anterior cutaneous nerves of abdomen, pectoral and abdominal anterior cutaneous branch of intercostal nerves. (05 Mar 2000) |
| anterior femoral cutaneous nerves | Anterior cutaneous branches of femoral nerve; supplies distal 3/4 of skin and superficial fascia of anterior and medial thigh. Synonym: rami cutanei anteriores nervi femoralis. (05 Mar 2000) |
| anthroponotic cutaneous leishmaniasis | A form of Old World cutaneous leishmaniasis, usually with a prolonged incubation period and confined to urban areas. Synonym: chronic cutaneous leishmaniasis, dry cutaneous leishmaniasis, urban cutaneous leishmaniasis. (05 Mar 2000) |
| candidiasis, cutaneous | Candidiasis of the skin manifested as eczema-like lesions of the interdigital spaces, perleche, or chronic paronychia. (12 Dec 1998) |
| vasculitis, allergic cutaneous | Vasculitis due to allergic reaction, marked by such cutaneous lesions as papules, macules, vesicles, urticarial wheals, purpura, and small ulcers, and accompanied by itching and usually a slight fever and malaise. (12 Dec 1998) |
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