Abstract
Purpose: To determine the incidence of 22q11.2 microdeletions in the adult survivors of correction of tetralogy of Fallot who have familial congenital heart disease. Methods: Patients who had survived a correction of tetralogy of Fallot between 1954 and 1974 and had affected family members were identified during a study of these long-term survivors. Fluorescence in situ hybridization analysis was performed using both the N 25 (Oncor) and TUPLE1(VYSIS) probes, mapped to 22q11.2. Results: One of 18 (5.6%) patients had a microdeletion within 22q11.2, including both N25 and TUPLE1. Conclusion: 22q11.2 microdeletions involving TUPLE1 and/or N25 are present in a minority of adults with familial tetralogy of Fallot.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 61-64 |
| Number of pages | 4 |
| Journal | Genetics in Medicine |
| Volume | 3 |
| Issue number | 1 |
| DOIs | |
| State | Published - 2001 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- 22q11.2 microdeletion
- Congenital heart disease
- Genetics
- Tetralogy of Fallot
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