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.
Patient stories
22q11.2 Deletion and Duplication Syndromes Patient Stories
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.