MeSH 搜索器

Hyperhomocysteinemia

Condition in which the plasma levels of homocysteine and related metabolites are elevated (>13.9 ╬╝mol/l). Hyperhomocysteinemia can be familial or acquired. Development of the acquired hyperhomocysteinemia is mostly associated with vitamins B and/or folate deficiency (e.g., PERNICIOUS ANEMIA, vitamin malabsorption). Familial hyperhomocysteinemia often results in a more severe elevation of total homocysteine and excretion into the urine, resulting in HOMOCYSTINURIA. Hyperhomocysteinemia is a risk factor for cardiovascular and neurodegenerative diseases, osteoporotic fractures and complications during pregnancy.
推出的年份: 1999
副标题
树号: C16.320.565.100.480, C18.452.603.378, C18.452.648.100.480, C18.654.521.500.133.699.418
MeSH 单一 ID: D020138
进入的组:
  • Hyperhomocysteinemias
早前的内容:
  • Homocysteine/blood (1991-1998)

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