| MASA | Medical Association of South Africa; mental retardation-aphasia-shuffling gait-adducted thumbs [synd... |
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| CHA | Canadian Hospital Association; Catholic Health Association; Chinese hamster; chronic hemolytic anemi... |
| FHA | familial hypoplastic anemia; Fellow of the Institute of Hospital Administrators; filamentous hemaggl... |
| HAL | hepatic artery ligation; hypoplastic acute leukemia |
| HLHS | hypoplastic left heart syndrome |
| HLHS | Hypoplastic left heart syndrome |
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| adducted thumbs with mental reatardation | A syndrome with the following characteristic features: (1) neurologically:mental retardation and aphasia (lack of speech); (2) limbs: adducted (clasped) thumbs, absent extensor pollicis longus and/or brevis muscles to the thumb, shuffling gait, and leg spasticity; (3) growth: small body size; (4) skeleton: lumbar lordosis (sway back). The syndrome is inherited as an X-linked trait and so affects mainly boys. Alternative names include MASA syndrome ( MASA stands for mental retardation, aphasia, shuffling gait, and adducted thumbs), clasped thumb and mental retardation, congenital clasped thumb with mental retardation, and the Gareis-Mason syndrome. (12 Dec 1998) |
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| clasped thumbs and mental retardation | A syndrome with the following characteristic features: (1) neurologically:mental retardation and aphasia (lack of speech); (2) limbs: adducted (clasped) thumbs, absent extensor pollicis longus and/or brevis muscles to the thumb, shuffling gait, and leg spasticity; (3) growth: small body size; (4) skeleton: lumbar lordosis (sway back). The syndrome is inherited as an X-linked trait and so affects mainly boys. Alternative names include MASA syndrome (MASA stands for mental retardation, aphasia, shuffling gait, and adducted thumbs), adducted thumb with mental retardation, congenital clasped thumb with mental retardation, and the Gareis-Mason syndrome. (12 Dec 1998) |
| hitchhiker thumbs | Malposition of the thumb's which as a result of shortness of the first metacarpal stand at right angles to the radial border of the hand and in the same place as it; a characteristic sign of diastrophic dwarfism. (05 Mar 2000) |
| congenital hypoplastic 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) |
| hypoplastic | Pertaining to or characterised by hypoplasia. (05 Mar 2000) |
| hypoplastic anaemia | <haematology> A low red blood cell count that results from the underproduction of red blood cells by the bone marrow. This is often secondary to a drug (chemotherapy) side effect. (27 Sep 1997) |
| hypoplastic foetal chondrodystrophy | A developmental error of the epiphyses characterised by severe deformities, epiphyses ossified from several discrete centres and with a stippled appearance, and thickened shafts of the long bones; congenital cataract and mental retardation are often present. There is an autosomal dominant form and an autosomal recessive form. Synonym: chondrodysplasia punctata, chondrodystrophia calcificans congenita, hypoplastic foetal chondrodystrophy, stippled epiphysis. (05 Mar 2000) |
| hypoplastic heart | A small heart, as seen in Addison's disease. (05 Mar 2000) |
| hypoplastic left heart syndrome | <syndrome> Underdevelopment of the left side of the heart characterised by: aortic valve atresia, hypoplastic ascending aorta, hypoplastic/atretic mitral valve, endocardial fibroelastosis most common cause of congestive heart failure in neonate, 25% of cardiac deaths in 1st week of life, prognosis: 100% fatal by 6 weeks haemodynamics: pulmonary venous return is diverted from LA to RA through atrial septal defect, RV supplies pulmonary artery, ductus arteriosus, descending aorta (antegrade flow), aortic arch, ascending aorta, coronary circulation (retrograde flow), leads to RV work overload and congestive heart failure Treatment: Norwood procedure (palliative), transplant (12 Dec 1998) |
| familial hypoplastic 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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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