假性骨弯曲畸形发育不良
Pseudodiastrophic dysplasia
ORPHA:85174疾病
定义 英文原文(暂无中文)
Pseudodiastrophic dysplasia is characterized by rhizomelic shortening of the limbs and severe clubfoot deformity, in association with elbow and proximal interphalangeal joint dislocations, platyspondyly, and scoliosis. It has been described in about 10 patients. An autosomal recessive inheritance has been suggested. Pseudodiastrophic dysplasia differs from diastrophic dysplasia on the basis of clinical, radiographic, and histopathologic findings. Clubfoot can be treated by surgical therapy, and neonatal contractures and scoliosis can be relieved by physical therapy. Several of the reported patients died in the neonatal period or during infancy.
基本事实
- 遗传方式
- 常染色体隐性
- 发病年龄
- 婴儿期、新生儿期
- 患病率
- <1 / 1 000 000
临床表型 9
极常见 99–80%7
- 肘关节脱位 HP:0003042
- 颧骨扁平 HP:0000272
- 指(趾)骨错位 HP:0006243
- 扁平椎 HP:0000926
- 肢体近端缩短 HP:0008905
- 脊柱侧弯 HP:0002650
- 马蹄内翻足 HP:0001762
偶见 29–5%2
- 心血管系统形态异常 HP:0030680
- 脐膨出 HP:0001539
外部标识与链接
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本页数据来源
- 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
- 中文病名:Orphanet 中文包,冻结于 2020-06-01
- 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)