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III型atelosteogenesis:一种独特的骨骼发育不良,具有与atelosteogenesis和II型耳-腭-指综合征重叠的特征。

Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II.

作者信息

Stern H J, Graham J M, Lachman R S, Horton W, Bernini P M, Spiegel P K, Bodurtha J, Ives E J, Bocian M, Rimoin D L

机构信息

Medical Genetics-Birth Defects Center, Ahmanson Pediatrics Center, Cedars-Sinai Medical Center, UCLA School of Medicine 90048.

出版信息

Am J Med Genet. 1990 Jun;36(2):183-95. doi: 10.1002/ajmg.1320360212.

Abstract

We present 5 cases of a short-limb dwarfism syndrome whose manifestations overlap those of atelosteogenesis and oto-palato-digital syndrome Type II. Clinical, radiographic, genetic, and histologic data are presented which demonstrate differences between our patients and previously reported cases of these other conditions. We conclude that the disorder seen in these children represents a distinct chondrodysplasia for which we propose the name atelosteogenesis Type III.

摘要

我们报告了5例短肢侏儒综合征病例,其表现与atelosteogenesis和II型耳-腭-指综合征有重叠。本文展示了临床、影像学、遗传学和组织学数据,这些数据证明了我们的患者与先前报道的这些其他病症病例之间的差异。我们得出结论,这些儿童所患的疾病代表一种独特的软骨发育异常,我们提议将其命名为III型atelosteogenesis。

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