Dinno N D, Shearer L T, Weisskopf B
Pediatr Radiol. 1980 Feb;9(2):105-8. doi: 10.1007/BF00977673.
We report an unusual form of chondrodystrophy identified in a female infant at birth. She was severely delayed developmentally and expired at one year of age. The dwarfism was characterized by brachymelia, dysmorphic features and unusual radiologic findings of the extremities and thorax. The spine, hand and foot X-rays were normal. The clinical and radiologic manifestations are unique and unrelated to other described entities.
我们报告了一名女婴出生时被确诊的一种罕见的软骨发育不良形式。她发育严重迟缓,一岁时死亡。侏儒症的特征为短肢、畸形特征以及四肢和胸部不同寻常的放射学表现。脊柱、手部和足部的X光片正常。其临床和放射学表现独特,与其他已描述的病症无关。