Myocardial infarction from isolated coronary artery vasculitis in a young patient: A rare case
File version
Author(s)
Rahman, Atifur
Tai, Shayan
Hamilton-Craig, Ian
Hamilton-Craig, Christian
Griffith University Author(s)
Primary Supervisor
Other Supervisors
Editor(s)
Date
Size
File type(s)
Location
License
Abstract
Symptomatic coronary artery disease (CAD) primarily occurs in patients over the age of 40, however younger men and women can also be affected. The pathophysiology of CAD in this group is often not due to atherosclerotic plaque rupture, except for those with genetically predetermined risk such as familial hypercholesterolaemia. In an autopsy study of victims aged 15–34 years, advanced coronary atheromas were seen only in 2% of males aged 15–19 years, and none in females [ 1 ]. Many of these cases may have had severe heterozygous familial hypercholesterolaemia (FH), which occurs with a frequency of 1:300–1:500 of the general population, and in which total cholesterol levels are very high (usually > 8 mmol/L) [ 2 ].
Journal Title
International Journal of Cardiology
Conference Title
Book Title
Edition
Volume
180
Issue
Thesis Type
Degree Program
School
Publisher link
Patent number
Funder(s)
Grant identifier(s)
Rights Statement
Rights Statement
Item Access Status
Note
Access the data
Related item(s)
Subject
Cardiovascular medicine and haematology
Science & Technology
Life Sciences & Biomedicine
Cardiac & Cardiovascular Systems
Cardiovascular System & Cardiology
Acute coronary syndrome
Persistent link to this record
Citation
Markham, R; Rahman, A; Tai, S; Hamilton-Craig, I; Hamilton-Craig, C, Myocardial infarction from isolated coronary artery vasculitis in a young patient: A rare case, International Journal of Cardiology, 2015, 180, pp. 40-41