Suppr超能文献

胸壁畸形的病因——给治疗医生的遗传学综述

Etiology of chest wall deformities--a genetic review for the treating physician.

作者信息

Kotzot Dieter, Schwabegger Anton H

机构信息

Division of Clinical Genetics, Department of Medical Genetics, Molecular and Clinical Pharmacology, Innsbruck Medical University, A-6020 Innsbruck, Austria.

出版信息

J Pediatr Surg. 2009 Oct;44(10):2004-11. doi: 10.1016/j.jpedsurg.2009.07.029.

Abstract

Chest wall deformities such as pectus excavatum, pectus carinatum, and cleft sternum can be isolated malformations or dysmorphic features of genetic associations, monogenic disorders, and various numeric and structural chromosomal aberrations. In contrast to the most important syndromes such as Marfan syndrome or Noonan syndrome that can be associated with a chest wall deformity and for which the causative genes are known, etiology of isolated chest wall deformities is still a matter of research. Therefore, an interdisciplinary approach, particularly in patients with additional symptoms is strongly recommended to choose the best therapeutic approach for each patient and its family.

摘要

胸壁畸形,如漏斗胸、鸡胸和胸骨裂,可能是孤立的畸形,也可能是遗传关联、单基因疾病以及各种数量和结构染色体畸变的畸形特征。与可伴有胸壁畸形且致病基因已知的最重要综合征(如马凡综合征或努南综合征)不同,孤立性胸壁畸形的病因仍是一个研究课题。因此,强烈建议采用跨学科方法,尤其是对于有其他症状的患者,以便为每个患者及其家庭选择最佳治疗方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验