SPONDYLOMETEPIPHYSEAL DYSPLASIA-CONGENITA, STRUDWICK TYPE

被引：10

作者：

SHEBIB, SM

CHUDLEY, AE

REED, MH

机构：

[1] CHILDRENS HOSP,DEPT RADIOL,840 SHERBROOK ST,WINNIPEG B3A 1S1,MANITOBA,CANADA

[2] UNIV MANITOBA,DEPT RADIOL,WINNIPEG R3T 2N2,MANITOBA,CANADA

[3] UNIV MANITOBA,DEPT PEDIAT & CHILD HLTH,WINNIPEG R3T 2N2,MANITOBA,CANADA

[4] UNIV MANITOBA,DEPT HUMAN GENET,WINNIPEG R3T 2N2,MANITOBA,CANADA

来源：

PEDIATRIC RADIOLOGY | 1991年 / 21卷 / 04期

关键词：

D O I：

10.1007/BF02018630

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

A case of spondylometepiphyseal dysplasia congenita, Strudwick type is presented. At birth, this condition cannot be distinguished from spondyloepiphyseal dysplasia congenita. Features in common include delayed ossification of the pubic bones and proximal femoral epiphyses, coxa vara, odontoid hypoplasia and lumbar lordosis. The distinguishing radiologic feature of this condition is the striking irregularity of long bone metaphyses which develops during infancy.

引用

页码：298 / 300

页数：3

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