A healthy pregnancy is essential for delivering a healthy baby. Eating a nutritious diet helps with good fetal brain development, decreases birth defects and results in a healthy birth weight.
Unfortunately, you can have other complications like genetic abnormalities. Read on to find out how a diagnosis for skeletal dysplasias is made during pregnancy.
Talk About Family History
Skeletal dysplasias are made up of over 200 complex disorders. Each type has it own set of complex complications. This condition affects your cartilage growth and the fetal bone. It results in developing dwarfism or a short stature.
This condition occurs from genetic abnormalities and gene mutations. Skeletal dysplasias are often passed down through generations. If you have one child born with skeletal dysplasia, then it can occur in another pregnancy.
Get An MRI
You should tell your doctor about your family immediately. Skeletal dysplasia is usually not picked up by an ultrasound until at 20 weeks of the pregnancy. If the doctor suspects the condition is presented, then he will need an examination of the fetal skeleton. Your doctor can get this image by sending you to radiology in Toms River NJ.
A MRI will need to be done to get a look at the fetal skeleton for any abnormality. Your doctor also want to perform genetic testing. This testing is done when doctors suspect skeletal dysplasia before birth. It is also done when the patient does not have a family history of the disorder.
No Treatment Before Birth
A prenatal treatment is not available for skeletal dysplasias. However, your doctor will plan for your delivery. A post-natal care is also in place to make sure your newborn has a smooth transition.
It helps to take one step at a time. You should focus on having a healthy pregnancy. After the baby’s birth, you can schedule tests to confirm this condition.