22q11.2 Deletion and Duplication Syndromes Patient Stories
1 - 4 of 4
22q11.2 Deletion Syndrome: Jasmine's Story
Jasmine, 14, is thriving thanks to early intervention and continuing treatment and support from the 22Q and You Center at Children's Hospital of Philadelphia.
Tetralogy of Fallot (TOF): Alissa’s Story
When Alissa was a baby, she underwent heart surgery at Children’s Hospital of Philadelphia to treat tetralogy of Fallot (TOF), a congenital heart defect.
Lymphatic Leaks: Naelani’s Story
Naelani was flown from Texas to Children’s Hospital of Philadelphia for an innovative procedure which worked to seal her lymphatic leaks.
Chromosome 22q11.2 Deletion and Tetralogy of Fallot: Jack's Story
Born with a heart defect called tetralogy of Fallot, Jack was just 9 days old when his family learned he also had chromosome 22q11.2 deletion, a rare chromosomal difference.