单词 | embryopathy |
释义 | embryopathyem·bry·op·a·thyE0108100 (ĕm′brē-ŏp′ə-thē)Embryopathyembryopathy[‚em·brē′äp·ə·thē]Embryopathya disease of or injury to a human embryo occurring between the middle of the first and the end of the third month of intrauterine development. Embryopathy may be caused by a genetic disturbance or by a pathogenic factor that affects the embryo through the mother, such as hypoxia, poisoning, or an infectious disease. Embryopathy may result in malformation of embryonic organs, developmental anomalies, and spontaneous abortion. Prevention calls for the protection of the mother’s health during the first months of pregnancy. embryopathyembryopathy[em″bre-op´ah-the]em·bry·op·a·thy(em'brē-op'ă-thē),embryopathy(ĕm′brē-ŏp′ə-thē)embryopathyA general term for any constellation of malformations attributed to a particular exogenous agent. See AIDS embryopathy, Alcohol embryopathy, Diabetic embryopathy, Retinoic acid embryopathy, Varicella embryopathy, Vitamin A embryopathy.em·bry·op·a·thy(em'brē-op'ă-thē)Synonym(s): fetopathy. embryopathyAny developmental or biochemical disorder of an EMBRYO. |
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