Fitzsimmons-Guilbert syndrome

名词 n.

英文释义

名词 n.
  1. A rare genetic disorder characterized by slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal–phalangeal pattern profile, sternal anomaly (pectus carinatum or excavatum), dysarthria, and mild intellectual deficit. uncountable
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