| SLO | Smith-Lemli-Opitz syndrome; streptolysin O |
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| SLOS | Smith-Lemli-Opitz syndrome |
| SLO | Smith Lemli Opitz syndrome |
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| SLOS | Smith--Lemli--Opitz syndrome |
| SLO | Smith-Lemli-Opitz |
| Opitz | John M., U.S. Paediatrician, *1935. See: Smith-Lemli-Opitz syndrome. (05 Mar 2000) |
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| smith-lemli-opitz syndrome | <syndrome> Autosomal recessive disorder characterised by multiple congenital anomalies including microcephaly, mental retardation, unusual facies, and genital abnormalities. The biochemical defect is a lack of 7-dehydrocholesterol-delta-7-reductase, resulting in abnormally high levels of 7-dehydrocholesterol and low levels of cholesterol. (12 Dec 1998) |
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| Opitz syndrome |
Opitz-Frias syndrome; a genetic syndrome with hypertelorism (widely spaced eyes), hypospadias (genital abnormality in males), severe swallowing problems, and mental retardation in two thirds of cases. Inheritance is autosomal dominant.
출처: www.childrenwithchallenges.net/definitions/O.html
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| Opitz d. |
enlargement of the spleen due to thrombosis of the splenic vein; called also thrombophlebitic splenomegaly.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Opitz disease |
see under disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Opitz s. |
an autosomal dominant syndrome consisting of hypertelorism and hernias, and in males hypospadias, cryptorchidism, and bifid scrotum. Cardiac anomalies, laryngotracheal malformations, imperforate anus, renal defects, lung hypoplasia, and downslanted palpebral fissures may also be present. Called also G s. and hypertelorism-hypospadias s.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Opitz-Frias syndrome |
see under syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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