指屈曲-纤维组织增生-骨骼发育不良综合征
Camptodactyly-fibrous tissue hyperplasia-skeletal anomalies syndrome
ORPHA:1321疾病
定义 英文原文（暂无中文）
An extremely rare chondrodysplastic malformation syndrome characterized by the combination of arachnodactyly, becoming evident at around the age of 10, camptodactyly, and scoliosis. Additional reported manifestations include a mild intellectual disability and a mild facial dysmorphism including a broad nose and flaring nostrils. There have been no further descriptions in the literature since 1972.
别名
Goodman指弯曲畸形
基本事实
- 发病年龄
- 新生儿期
- 患病率
- <1 / 1 000 000
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）