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CHARACTERIZATION OF ENZYME DEFECTS IN PORPHYRIAS

CHARACTERIZATION OF ENZYME DEFECTS IN PORPHYRIAS
卟啉症酶缺陷的表征
批准号:
6276386
负责人:
KARL E ANDERSON
金额:
$2.69万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-12-01 至 1998-11-30

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项目成果

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中文摘要
翻译
其目的是确定已知或已知的患者的酶缺陷。 疑似卟啉症及其家人。方法包括测量 红细胞中胆红素原脱氨酶和卟啉、卟啉和 卟啉前体(β-氨基酮丙酸和卟啉原) 血浆和尿液,以及粪便中的卟啉。录入选定的患者 在该机构和其他机构的其他卟啉病研究方案中, 包括分析DNA以确定血红素基因的特定突变 生物合成途径酶。
英文摘要
The purpose is to characterize enzyme defects in patients with known or suspected porphyria and their families. Methods include measurement of porphobilinogen deaminase and porphyrins in erythrocytes, porphyrins and porphyrin precursors (delta-aminolevulinic acid and porphobilinogen) in plasma and urine, and porphyrins in feces. Selected patients are entered in other porphyria research protocols at this and other institutions, including analysis of DNA to identify specific mutations in genes for heme biosynthetic pathway enzymes.
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CHARACTERIZATION OF ENZYME DEFECTS IN PORPHYRIAS
STUDIES IN PORPHYRIA III, HEME, AND TIN MESOPORPHYRIN IN ACUTE PORPHYRIAS
HEME ARGINATE IN ACUTE PORPHYRIA
STUDIES IN PORPHYRIA CUTANEA TARDA
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