| ¿µ¹® | transient ischemic attack(TIA) | ÇÑ±Û | Àϰú¼ºÇãÇ÷¹ßÀÛ |
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| ¿µ¹® | red bone marrow | ÇÑ±Û | Àû»ö°ñ¼ö |
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| ¿µ¹® | acquired immunodeficiency syndrome | ÇÑ±Û | ÈÄõ¸é¿ª°áÇÌÁõÈıº, ¿¡ÀÌÁî |
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| ¿µ¹® | white blood cell(WBC), leukocyte | ÇÑ±Û | ¹éÇ÷±¸ |
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| CAPRCA | chronic, acquired, pure red cell aplasia |
|---|---|
| PRCA | Pure Red Cell Aplasia |
| CPRCA | constitutional pure red cell aplasia |
| PRCA | pure red cell aplasia |
| RC | an electronic circuit containing a resistor and capacitor in series; radiocarpal; reaction center; r... |
| PRCA | Pure Red Cell Aplasia |
|---|---|
| ACC | Aplasia cutis congenita |
| CP | Commercially pure |
| CP Ti | Commercially pure titanium |
| IUPAC | International Union of Pure and Applied Chemistry |
| red-cell aplasia, pure | Suppression of erythropoiesis with little or no abnormality of leukocyte or platelet production. (12 Dec 1998) |
|---|---|
| pure red cell aplasia | A transitory arrest of red blood cell production which may occur in the course of a haemolytic anaemia, often preceded by infection, or as a complication of certain drugs; if the arrest persists anaemia may result. See: congenital hypoplastic anaemia. (05 Mar 2000) |
| pure red cell anaemia | Congenital nonregenerative, familial hypoplastic, or pure red cell anaemia; erythrogenesis imperfecta; Diamond-Blackfan syndrome; autosomal recessive normocytic normochromic anaemia resulting from congenital hypoplasia of the bone marrow, which is grossly deficient in erythroid precursors while other elements are normal; anaemia is progressive and severe, but leukocyte and platelet counts are normal or slightly reduced; survival of transfused erythrocytes is normal; minor congenital anomalies are found in some patients. Synonym: congenital nonregenerative anaemia, Diamond-Blackfan anaemia, Diamond-Blackfan syndrome, erythrogenesis imperfecta, familial hypoplastic anaemia, pure red cell anaemia. (05 Mar 2000) |
| aplasia | <embryology> A lack of development of an organ or tissue or of the cellular products from an organ or tissue. Compare: hypoplasia. Origin: Gr. Plassein = to form (18 Nov 1997) |
| aplasia cutis congenita | Congenital absence or deficiency of a localised area of skin, with the base of the defect covered by a thin translucent membrane; most often a single area near the vertex of the scalp, but may occur in other areas; underlying structures may also be affected; autosomal inheritance, either dominant or recessive. (05 Mar 2000) |
| radial aplasia-thrombocytopenia syndrome | <syndrome> Aplasia (absence) of the radius (the long bone on the thumb-side of the forearm) and thrombocytopenia (low blood platelets) are key features characterizing this syndrome. There is phocomelia (flipper-limb) with the thumbs always present. The fibula (the smaller bone in the lower leg) is often absent. The risk of bleeding from too few platelets is high in early infancy but lessens with age. The condition is inherited in an autosomal recessive trait with one gene (on a non-sex chromosome) coming from each parent to the child affected with the disease. Alternative names include thrombocytopenia-absent radius syndrome, tar syndrome, and tetraphocomelia-thrombocytopenia syndrome. (12 Dec 1998) |
| germinal aplasia | A disorder in which the seminiferous tubules exhibit an abnormal cytoarchitecture and extensive hyalinization; the testes are small, and few spermatozoa are formed; the body habitus may be eunuchoid, and gynaecomastia may be present; urinary gonadotropin output is usually high, and the incidence of mental deficiency and illness increased; sex chromatin may be male or female, and androgen secretion ranges from subnormal to normal. It is a constant feature of (and is often used synonymously with) Klinefelter's syndrome. Synonym: germinal aplasia. (05 Mar 2000) |
| gonadal aplasia | Congenital absence of essentially all gonadal tissue; the external genitalia and genital ducts are female, but if interstitial cells of Leydig are present, the external genitalia are commonly ambiguous and the genital ducts are female. See: gonadal dysgenesis. Compare: Klinefelter's syndrome, Turner's syndrome. Synonym: gonadal agenesis. (05 Mar 2000) |
| congenital aplasia of thymus | diGeorge syndrome |
| syndrome, radial aplasia-thrombocytopenia | See syndrome, tar. (12 Dec 1998) |
| thymic aplasia | <disease, immunology> A lack of T lymphocytes, due to failure of the thymus to develop, resulting in very reduced cell-mediated immunity though serum immunoglobulin levels may be normal. See: DiGeorge syndrome. Origin: Gr. Plassein = to form (18 Nov 1997) |
| cerebral ischemia, transient | Nonconvulsive, reversible, focal neurologic deficits lasting minutes up to about 24 hours, resulting mainly from arteriosclerosis, emboli, or hypertensive episodes. (12 Dec 1998) |
| transient | 1. Short-lived; passing; not permanent; said of a disease or an attack. 2. A short-lived cardiac sound having little duration (less than 0.12 second) as distinct from a murmur; e.g., first, second, third, and fourth heart sounds, clicks, and opening snaps. Origin: L. Transeo, pres. P. Transiens, to cross over (05 Mar 2000) |
| transient acantholytic dermatosis | A pruritic papular eruption, with histologic suprabasal acantholysis, of the chest, with scattered lesions of the back and lateral aspects of the extremities, lasting from a few weeks to several months; seen predominantly in males over 40. Synonym: Grover's disease. (05 Mar 2000) |
| transient agammaglobulinaemia | A type of primary immunodeficiency that occurs in infants of both sexes, usually before the sixth month of life, probably resulting from immaturity of lymphoid tissue. Synonym: transient agammaglobulinaemia. (05 Mar 2000) |
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