Engelmann's disease with optic atrophy

被引：2
|
作者：
Soni J.P. [1 ]
Gupta B.D. [1 ]
Soni M. [1 ]
Mund V. [1 ]
Aneja R. [1 ]
机构：
[1] Madhu Kunj, Jodhpur-342001, 23G, In Front of Railway Med. Colony
来源：
The Indian Journal of Pediatrics | 2002年 / 69卷 / 9期
关键词：
Diaphyseal; Endosteal; Epiphysis; Metaphysis;
D O I：
10.1007/BF02723700
中图分类号：
学科分类号：
摘要：
Engelman - Camurati disease is a rare Diaphyseal dysplasia, characterized by endosteal and periostal thickness of cortex of shaft of tubular bone sparing metaphysis and epiphysis. The bone of the hand, feet, ribs, scapulae and pubis are not affected.
引用
收藏
页码：823 / 824
页数：1
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