Genetic background
Apert syndrome is an autosomal dominant condition, meaning that only one parent needs to have
an abnormal gene for the child to inherit the disease ( genotype AA.) Yes, Apert syndrome is genetic.
Children with Apert Syndrome also have other birth defects.This condition is shown as a incomplete
dominants.
Incomplete Dominates means one allele and the dominate over powers the recessive allele
an abnormal gene for the child to inherit the disease ( genotype AA.) Yes, Apert syndrome is genetic.
Children with Apert Syndrome also have other birth defects.This condition is shown as a incomplete
dominants.
Incomplete Dominates means one allele and the dominate over powers the recessive allele