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MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 1 ÆäÀÌÁö: 1
  • Smith-Lemli-Opitz Syndrome - »õâ An autosomal recessive disorder of CHOLESTEROL metabolism. It is caused by a deficiency of 7-dehydrocholesterol reductase (DHCR7), the enzyme that converts 7-dehydrocholesterol to cholesterol, leading to an abnormally low plasma cholesterol. This syndrome is characterized by multiple CONGENITAL ABNORMALITIES, growth deficiency, and MENTAL RETARDATION.
    Synonyms : RSH-SLO Syndrome, Smith-Lemli-Opitz Syndrome, Type I, Smith-Lemli-Opitz Syndrome, Type II, RSH SLO Syndrome, RSH Syndromes, RSH-SLO Syndromes, Smith Lemli Opitz Syndrome, Smith Lemli Opitz Syndrome, Type I, Smith Lemli Opitz Syndrome, Type II
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MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 1
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