Apert Syndrome: Causes, Symptoms & Treatment

Apert syndrome is a rare hereditary disease. Malformations occur throughout the organism with severe, chronic loss of function and disease progression through deformities. Both sexes are equally affected. What is Apert syndrome? Apert syndrome, also known as acrocephalosyndactyly syndrome, is causative of severe to very severe malformations that can affect the entire body. These multiple … Apert Syndrome: Causes, Symptoms & Treatment

Isolated Lissencephaly: Causes, Symptoms & Treatment

Isolated lissencephaly is a congenital maldevelopment of the brain caused by a genetic defect. This leads to very severe physical and mental disabilities in affected children. Isolated lissencephaly is very rare. What is isolated lissencephaly? Isolated lissencephaly is a congenital developmental disorder of the human brain and is one of the five forms of lissencephaly. … Isolated Lissencephaly: Causes, Symptoms & Treatment