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Fragile X Syndrome
It tests for 550 genetic diseases that can affect children
plus an extended panel for both reproductive partners with a combined report looking at 100's of other inherited conditions
Comprehensive carrier screening is an at-home genetic test that checks to see if you have a higher chance of having a baby with a serious genetic disease
We also include a free chat with a genetic counsellor if they'd like help figuring out what test is right for them
Carrier Screening with Newlife IVF heart Fragile X SyndromeComprehensive carrier screening is an at home genetic test that checks to see if you have a higher chance of having a baby with a serious inherited genetic disease. It tests for up to 343 genetic diseases that can affect children, including cystic fibrosis, spinal muscular atrophy, Tay Sachs Disease, and fragile X syndrome.
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