Abstract
Our results confirm that classic TF can be associated with many genetic conditions, but most patients are nonsyndromic. In contrast, children with TF-PA have a high incidence of genetic syndromes, particularly those related to CATCH22 syndrome.
MeSH terms
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Abnormalities, Multiple / epidemiology
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Abnormalities, Multiple / genetics*
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Case-Control Studies
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Child, Preschool
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Chromosome Deletion*
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Chromosomes, Human, Pair 22*
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Female
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Heart Septal Defects, Ventricular / genetics*
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Humans
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Incidence
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Male
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Prevalence
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Pulmonary Atresia / genetics*
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Syndrome
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Tetralogy of Fallot / genetics*