Back to Search Start Over

Familial pneumothorax: towards precision medicine.

Authors :
Scott RM
Henske EP
Raby B
Boone PM
Rusk RA
Marciniak SJ
Source :
Thorax [Thorax] 2018 Mar; Vol. 73 (3), pp. 270-276. Date of Electronic Publication: 2017 Dec 28.
Publication Year :
2018

Abstract

One in 10 patients suffering from primary spontaneous pneumothoraces has a family history of the disorder. Such familial pneumothoraces can occur in isolation, but can also be the presentation of serious genetic disorders with life-threatening vascular or cancerous complications. As the pneumothorax frequently precedes the more dangerous complications by many years, it provides an opportunity to intervene in a focused manner, permitting the practice of precision medicine. In this review, we will discuss the clinical manifestations and underlying biology of the genetic causes of familial pneumothorax.<br />Competing Interests: Competing interests: None declared.<br /> (© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.)

Details

Language :
English
ISSN :
1468-3296
Volume :
73
Issue :
3
Database :
MEDLINE
Journal :
Thorax
Publication Type :
Academic Journal
Accession number :
29288214
Full Text :
https://doi.org/10.1136/thoraxjnl-2017-211169