diaphyseal

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di·aph·y·sis

 (dī-ăf′ĭ-sĭs)
n. pl. di·aph·y·ses (-sēz′) Anatomy
The shaft of a long bone.

[Greek diaphusis, spinous process of the tibia, from diaphuesthai, to grow between : dia-, dia- + phuesthai, to grow, middle voice of phuein; see bheuə- in Indo-European roots.]

di′a·phys′i·al (dī′ə-fĭz′ē-əl), di·aph′y·se′al (dī-ăf′ĭ-sē′əl, dī′ə-fĭz′ē-əl) adj.
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Adj.1.diaphyseal - relating to the diaphysis of a bone
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References in periodicals archive ?
Progressive diaphyseal dysplasia, also known as Camurati-Engelmann disease (CED), is a rare autosomal dominant bone disorder caused by mutations in the transforming growth factor beta 1 (TGF- [beta]1) gene and characterized by cortical thickening of the diaphysis of tubular bones with sparing of the epiphysis and low bone mineral density.
Camurati-Engelmann disease (CED), or progressive diaphyseal dysplasia, is a rare sclerosing dysplasia of which 250 cases have been described in the English literature.
Camurati-Engelmann disease, or progressive diaphyseal dysplasia, is a rare sclerosing dysplasia.