Facio-cardio-cutaneous syndrome is a rare, genetic disorder that affects the skin, heart and blood vessels. It can cause facial abnormalities, heart defects and neurological problems. Facio-cardio-cutaneous syndrome is inherited in an autosomal dominant manner, which means that only one copy of the mutated gene from each parent is required for a child to inherit the disorder.The symptoms of facio-cardio-cutaneous syndrome vary from  Read More

Jervell and Lange-Nielsen syndrome is a rare genetic illness characterized by congenital deafness that occurs in conjunction with anomalies in the heart's electrical system. The severity of JLNS-related cardiac symptoms varies among individuals. Some people have no symptoms (asymptomatic); others develop abnormally fast heartbeats (tachyarrhythmias), which can cause bouts of unconsciousness, cardiogenic shock, and potential  Read More