No. Newborns have been screened for inherited disorders in the U.S. since the early 1960s. Every state currently maintains a screening program, but most states screen for no more than ten disorders and some for as few as four.
MoreIf my baby has a metabolic disorder, could my other children have it as well?
This question can best be answered by your physician or a trained genetic counselor. Many families seek genetic counseling to better understand why their baby has a particular disorder and to learn if any other family members could be at risk...
MoreHow many disorders does StepOne® panel include?
StepOne® can identify the presence of more than 50 inherited disorders, including Cystic Fibrosis, Maple Syrup Urine Disease, and Congenital Adrenal Hyperplasia as well as many lesser-known disorders your state may not include in its screening...
MoreHow is my baby tested?
A healthcare professional will draw a small sample of blood by pricking your baby’s heel. The sample is placed on the absorbent filter paper located in every StepOne® packet and sent to PerkinElmer Genetics’ laboratory for analysis.
MoreHow common are metabolic disorders?
One in 1,500 babies will be affected by a disorder that PerkinElmer Genetics can identify.Screening, diagnosis, and intervention within the first days of life are essential. Most of these disorders can be managed if treatment begins early. More...
MoreCan metabolic disorders be cured?
Metabolic disorders are part of an individual’s genetic makeup, so they cannot be “cured.” Early identification of a metabolic disorder can allow your physician to start specialized medical treatment that may improve the long-term health of your...
MoreCan I test my baby myself?
No. Your physician must coordinate the entire process. You should not, under any circumstances, attempt to draw and submit the blood sample yourself.
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