saethre-chotzen syndrome

Saethre-Chotzen Syndrome: Causes, Symptoms & Treatment

Saethre-Chotzen syndrome is a disease associated with craniosynostosis. Saethre-Chotzen syndrome is congenital, as the causes are genetic. The disease is referred to by the abbreviation SCS. The main symptoms of Saethre-Chotzen syndrome are synostosis of the cranial suture on one or both sides, ptosis, an asymmetrical face, unusually small ears, and strabismus. What is Saethre-Chotzen … Saethre-Chotzen Syndrome: Causes, Symptoms & Treatment

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