Aortopulmonary septal defect
Aortopulmonary septal defect | |
---|---|
Classification and external resources | |
Specialty | medical genetics |
ICD-10 | Q20.0-Q20.3, Q21.4 |
ICD-9-CM | 745.0-745.1 |
MeSH | D001028 |
An aortopulmonary septal defect is a group of rare congenital heart disorders that result from errors in the development of the aorticopulmonary septum.
There are numerous types.[1] Types include:
- persistent truncus arteriosus[2]
- double outlet right ventricle
- transposition of the great vessels
- tetralogy of Fallot
References
- ↑ McElhinney DB, Reddy VM, Tworetzky W, Silverman NH, Hanley FL (January 1998). "Early and late results after repair of aortopulmonary septal defect and associated anomalies in infants <6 months of age". Am. J. Cardiol. 81 (2): 195–201. doi:10.1016/S0002-9149(97)00881-3. PMID 9591904.
- ↑ "Cardiovascular Pathology". Retrieved 2007-10-14.
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