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单词 trisomy 18 syndrome
释义 trisomy 18 syndrome
[`trī´sō·mē `ā¦tēn ´sin´drōm]
MEDICINE
A congenital disorder due to trisomy of all or a large part of chromosome 18, characterized by severe mental deficiency, hypertonicity with clenched hands, and anomalies of the hands, sternum, pelvis, and facies; most infants so afflicted fail to thrive. Also known as Edwards' syndrome; E trisomy.
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