Hypertrophic cardiomyopathy is an inherited cardiac condition that can present with symptoms such as chest pain, shortness of breath on exertion, syncope and even sudden cardiac death.

Cases of hypertrophic cardiomyopathy in infants may have one of a number of genetic causes.

Many cases of cardiomyopathy in children will have an identifiable genetic cause.

Many cases of cardiomyopathy in young people will have an identifiable genetic cause.

Hypertrophic cardiomyopathy in children may have one of a number of genetic causes.

Noonan syndrome is typically inherited in an autosomal dominant pattern and can present pre- or postnatally with a range of clinical features, including raised nuchal translucency, congenital heart disease, early feeding difficulties, short stature and distinct facial features.