Population-based assessment of familial inheritance and neurologic comorbidities among patients with an isolated atrial septal defect

Congenital Heart Disease

Volumn 4, Issue 6, 2009, Pages 459-463

  Steenblik, Matthew H ^a   Mineau, Geraldine P ^b   Pimentel, Richard ^b   Michaels, Andrew D ^c  

^a Department of Medicine ^*  (United States)

^b UNIVERSITY OF UTAH   (United States)

^c UNIVERSITY OF UTAH   (United States)

Author keywords

Atrial septal defect; Familial inheritance; Genetics; Patent foramen ovale

Indexed keywords

ARTERY BYPASS; ARTICLE; CHILD; COMORBIDITY; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; GENETIC RISK; HEART ATRIUM SEPTUM DEFECT; HUMAN; MALE; MIGRAINE; NEUROLOGIC DISEASE; PEDIGREE; PRIORITY JOURNAL; SIBLING; STROKE; TRANSIENT ISCHEMIC ATTACK;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CEREBROVASCULAR DISORDERS; CHILD; CHILD, PRESCHOOL; COMORBIDITY; DATABASES, FACTUAL; FEMALE; FORAMEN OVALE, PATENT; GENETIC PREDISPOSITION TO DISEASE; HEART SEPTAL DEFECTS, ATRIAL; HUMANS; INFANT; INFANT, NEWBORN; ISCHEMIC ATTACK, TRANSIENT; MALE; MIDDLE AGED; MIGRAINE DISORDERS; RISK FACTORS; SIBLINGS; STROKE; YOUNG ADULT;

EID: 71149096483     PISSN: 1747079X     EISSN: 17470803     Source Type: Journal    
DOI: 10.1111/j.1747-0803.2009.00340.x     Document Type: Article

References (9)

1. Hagen P, Scholts D, Edward W. Incidence and size of patent foramen ovale during the first decade of life: an autopsy study of 965 normal hearts. Mayo Clin Proc 1984, 59:17-20.
2. Lechat P, Mas JL, Lascault G. Prevalence of patent foramen ovale in patients with stoke. N Engl J Med 1988, 318:1148-1152.
3. Di Tullio M, Sacco R, Gopal A, Mohr JP, Homma S. Patient foramen ovale as a risk factor for cryptogenic stoke. Ann Inten Med 1992, 117:461-465.
4. Bai Y, Sherman S, Khoury MJ, Flanders WD. Bias associated with study protocols in epidemiologic studies of diease familial aggregation. Am J Epidemiol 2000, 151:927-937.
5. Kerber RA. Method for calculating risk associated with family history of disease. Genet Epidemiol 1995, 12:291-301.
6. Clark KL, Yutzey KE, Benson DW. Transcription factors and congenital heart defects. Annu Rev Physiol 2006, 68:97-121.
7. Caputo S, Capozzi G, Russo MG. Familial recurrence of congenital heart disease in patients with ostium secundum atrial septal defect. Eur Heart J 2005, 26:2179-2184.
8. Wilmhurst PT, Pearson MJ, Nightingale S, Walsh KP, Morrison WL. Inheritance of persistent foramen ovale and atrial septal defects and the relation to familial migraine with aura. Heart 2004, 90:1315-1320.
9. Arquizan C, Coste J, Touboul PJ, Mas JL. Is patent foramen ovale a family trait? A transcranial Doppler sonographic study. Stroke 2001, 32:1563-1566.