Tessier 7型面裂
Tessier number 7 facial cleft
ORPHA:141276疾病
定义 英文原文（暂无中文）
A rare lateral facial cleft characterized by a temporo-zygomatic defect, usually with absence of the zygomatic arch and deformities of the mandibular ramus, condyle, and coronoid process. Associated soft tissue abnormalities include malformations of the ear and hypoplasia or absence of the temporal muscle. Preauricular hair may be absent or divided into two portions. Facial manifestations include macrostomia (with extension of the cleft to the corner of the mouth) and pre-auricular tags. Incomplete clefts may be found in the molar region and between the maxillary tuberosity and pterygoid process.
别名
联合性面裂
基本事实
- 遗传方式
- 常染色体显性
- 发病年龄
- 产前、新生儿期
相关基因 2
| 基因 | 名称 | 关联类型 |
|---|---|---|
| PTCH2 | patched 2 | Disease-causing germline mutation(s) in |
| SPECC1L | sperm antigen with calponin homology and coiled-coil domains 1 like | Disease-causing germline mutation(s) in |
外部标识与链接
发现这一页有错误？告诉我 · 邮件主题会自动带上本页的 ORPHA 编号
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）