Congenital disorders

Apert Syndrome is a rare genetic disorder that affects craniofacial and limb development. Apert Syndrome, also known as...

Hirschsprung's disease is a congenital disorder of the large intestine (colon) characterized by the absence of nerve cells in the lower...

Photo Credit: Adobe Stock Cri du Chat Syndrome, also known as 5p- syndrome, is a rare genetic disorder that is characterized by a...

© Paley Foundation 2017 Tibial hemimelia is a rare congenital disorder that affects the development of the lower leg. It is characterized...