Tm Bioscience to supply Oklahoma State's newborn screening program
"Oklahoma is one of a growing number of U.S. States incorporating genetic testing into their newborn screening programs. This trend creates a significant market opportunity for our CFTR ASR*, which competitively address the needs of this market," said Greg Hines, President and CEO of Tm Bioscience. The NSP is a collaborative program between Family Health Services and the Public Health Laboratory at the Oklahoma State Department of Health. All babies born in Oklahoma are screened for congenital hypothyroidism, galactosemia, phenylketonuria (PKU), sickle cell disease, and since Feb.14, 2005, cystic fibrosis and congenital adrenal hyperplasia. Each year the NSP laboratory screens approximately 50,000 infants and provides comprehensive follow-up services to ensure repeat testing is achieved for 1,300 newborns identified at risk for a disorder or genetic trait condition. Approximately 40 newborns are identified with a disorder annually and receive comprehensive follow services to ensure treatment and referral to pediatric subspecialty is achieved promptly. To promote the health of Oklahoma infants, the NSP is continuing to expand the screening test panel for the genetic disorder medium chain acyl-CoA dehydrogenase deficiency (MCAD).
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