Apert Syndrome Life Expectancy

A genetic disease in which the seams between the skull bones get closer than normal is known as apert syndrome.Head and
face are effected by this disease.

This is a gene defect which is caused by mutation in a gene which is called fibroblast growth
factor receptor 2.This condition is also known as cranisynostosis.

This disease is recognized by a skull x-ray and physical exam. X-ray of hand and foot are also
very important to determine the bone problems.

Apert syndrome life expectancy is very complicated. Other birth defects may exist.

Apert Syndrome life expectanacy has following symptoms:

Loss of Weight
Excessive Cough
Normal Fever
Regular Sneezing
Body Sickness

Hope this short article will help you to learn about apert syndrome life expectancy.