A CASE OF BILATERAL DYSPLASIA EPIPHYSEALIS HEMIMELICA ASSOCIATED WITHPOLYDACTYLY AND SYNDACTYLY

Citation
Y. Takegami et H. Nogami, A CASE OF BILATERAL DYSPLASIA EPIPHYSEALIS HEMIMELICA ASSOCIATED WITHPOLYDACTYLY AND SYNDACTYLY, Clinical orthopaedics and related research, (296), 1993, pp. 307-309
Citations number
9
Categorie Soggetti
Surgery,Orthopedics
ISSN journal
0009921X
Issue
296
Year of publication
1993
Pages
307 - 309
Database
ISI
SICI code
0009-921X(1993):296<307:ACOBDE>2.0.ZU;2-K
Abstract
Dysplasia epiphysealis hemimelica (DEH) on bilateral medial malleoli o ccurred in a boy who had polydactylies and syndactylies of all four li mbs. Cases with both bilateral and symmetrical DEH affection as in thi s case seem not to have been re ported previously in the literature. D ysplasia epiphysealis hemimelica complicated by congenital anomalies i s extremely rare. A one-month-old boy of normal delivery had polydacty lies of thumbs, small fingers, and great toes, and had symmetrical syn dactylies of fingers and toes. At age eight, the patient reported swel ling and tenderness on bilateral medial malleoli. Radiographs showed s mall blotches of radiopacity. Two years later, the radiopacities had e nlarged to become typical of DEH.