Log in

Newborn Screening

Please bare with us... this page is still under construction

To view the full document from the above page was pulled from please see "Timing is Everything" published by Network of Rare Blood Disorder Organizations (website: )

From the Museum of disABILITY in Buffalo NY - The  Guthrie Test - History of the Bloodspots

Across Canada - Please note, clicking the links below will take you to another website and off of CanPKU+'s website.

An example from British Columbia. Please note, each province may cover their own list of disorders

Around the World

Key Players in Newborn Screening History

Dr. Robert Guthrie

the “father of newborn screening.” Born June 28, 1916

You Tube Videos


When did newborn screening start in Canada?

NBS in Canada originated in the 1960s, shortly after Guthrie introduced the concept of PKU screening. Canada is the second largest geographical country in the world and has a population of 35.19 million

Is genetic screening legal in Canada?

Canadian law now prohibits any person from requiring an individual to undergo a genetic test or to disclose the existing results of genetic tests. Essentially, the Genetic Non-Discrimination Act puts you in control of your personal information.

Is newborn screening mandatory in Canada?

Health care providers are responsible for ensuring that all babies born in Canada are offered newborn screening. This screening identifies babies who need more testing. It does not provide a diagnosis. Screening is considered to be the standard of care for every baby but is not mandatory. For those with PKU they are born perfectly normal (with a broken enzyme) without being identified via this testing - they can be irreversibly damaged before being identified.

2021 © Copyright CanPKU.ORG


260 Adelaide Street East, #180
Toronto, ON, M5A 1N1, Canada
Toll Free: 1-877-226-7581

Powered by Wild Apricot Membership Software