Marfan's syndrome: a review
(2001) In Hospital Medicine 62(3). p.153-157- Abstract
- Marfan's syndrome is an inherited disorder of connective tissue, in which the most pronounced abnormalities occur in the musculoskeletal, cardiovascular and ocular systems. Aortic dilatation and dissection are the major causes of morbidity and mortality. Recent advances in surgical techniques and earlier intervention have reduced postoperative mortality and morbidity.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1120927
- author
- Aburawi, Elhadi LU ; O'Sullivan, J and Hasan, A
- publishing date
- 2001
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Hospital Medicine
- volume
- 62
- issue
- 3
- pages
- 153 - 157
- publisher
- Mark Allen
- external identifiers
-
- pmid:11291465
- scopus:0035291876
- ISSN
- 1462-3935
- language
- English
- LU publication?
- no
- id
- 074196f9-998f-4567-86a4-2577a7dcf787 (old id 1120927)
- date added to LUP
- 2016-04-01 15:57:01
- date last changed
- 2022-01-28 08:16:55
@article{074196f9-998f-4567-86a4-2577a7dcf787,
abstract = {{Marfan's syndrome is an inherited disorder of connective tissue, in which the most pronounced abnormalities occur in the musculoskeletal, cardiovascular and ocular systems. Aortic dilatation and dissection are the major causes of morbidity and mortality. Recent advances in surgical techniques and earlier intervention have reduced postoperative mortality and morbidity.}},
author = {{Aburawi, Elhadi and O'Sullivan, J and Hasan, A}},
issn = {{1462-3935}},
language = {{eng}},
number = {{3}},
pages = {{153--157}},
publisher = {{Mark Allen}},
series = {{Hospital Medicine}},
title = {{Marfan's syndrome: a review}},
volume = {{62}},
year = {{2001}},
}