The Apert symptom is a gene slight defect and belongs to the craniofacial anomaly the broad classification. The chances of having another child with Apert Syndrome is almost non-existent if both parents are unaffected. If one parent has Apert Syndrome, there is a chance that his children will have Apert Syndrome. Individuals with Apert syndrome have webbed or fused fingers and toes. The severity.....
