catecholaminergic polymorphic ventricular tachycardia 5

A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the TRDN gene on chromosome 6q22.

Signs and symptoms

• Premature ventricular contraction
• Polymorphic ventricular tachycardia
• Cardiac arrest
• Shock
• Proximal muscle weakness
• Syncope
• Prolonged QT interval

Also known as: CVPT5