At birth, Eli was diagnosed with Phenylketonuria (PKU), that is, he lacks an enzyme in his liver that does not properly break down the amino acid, phenylalanine, commonly found in proteins.
Author Archives: Webadmin Biotech
Metascreen
Screening is key to prevention of silent killers – Medium Chain acyl-CoA dehydrogenase deficiency (MCAD)
11
May
May
This story is shared by a family who lost a child to MCAD – Ben’s family .
11
May
May
Baby Lina was warded in the neonatal intensive care unit after showing signs of muscle weakness, low breathing rate, low cortisol, poor feeding and dehydration (dehydration).
11
May
May
Corrigan, now 7, enjoys his time splashing in the inflatable pool, something his parents never knew possible. As soon after birth, he was diagnosed with Citrullinemia.