Hello, Thank you for answering previous posts for myself. I have a question about my son who is 3 who has apparently inherited hcm from me. At age 2 he had an
ekgAtrioventricular block, ekg tracing
Ecg
Exercise stress test which showed left
ventricularParoxysmal supraventricular tachycardia (psvt)
Ultrasound, ventricular septal defect - heartbeat
Ventricular assist device
Ventricular fibrillation
Ventricular septal defect
Ventricular tachycardia hypertrophyEnlarged prostate
Lymphoid hyperplasia. An echo at that time revealed a
normalNormal saline flush heart, with a lv measruement in the high
normalNormal saline flush range. 16 months later, at age 3 he had a repeat
ekgAtrioventricular block, ekg tracing
Ecg
Exercise stress test, which still showed lvh. The echo, however, showed IHSS with the septal measurement at the thickest point being 18 millimeters. A holter monitor (boy that was a fun experience!) revealed no arrythmia. He will have repeat echo's every 6 months. Is this extremely serious? Everything I have read states that hcm usually doesn't present until puberty. Also, with this septal measurment, does my son need to be seen by someone who specializes in pediatric hypertrophic cardiomyopathy, or is he ok being followed by a regular pediatric cardiologist? As far as I know, he has no symptoms - he runs around and plays like any normal 3 year old.
Thank you so much for answering my posts.
Barbara