Apert syndrome is a rare genetic disorder that primarily affects the development of the skull, face, and limbs. It is characterized by craniosynostosis (premature fusion of the skull bones), which leads to various facial abnormalities such as a sunken appearance of the midface, bulging eyes, and a prominent forehead. The condition also causes syndactyly, which is the fusion of fingers and toes. Congenital heart defects, such as atrial septal defects or ventricular septal defects, can also be present in some individuals with Apert syndrome. Therefore, the correct answer is miscarriage, cancer, congenital heart defects, and facial abnormalities.
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The answer is miscarriage, cancer, congenital heart defects, and facial abnormalities.
It could only be one.
I apologize for the confusion. The main characteristic of Apert syndrome is facial abnormalities.
