Kashaf Alkawashef

ALKAWASHEF : Clinical chemistry

PKU PHENYLKETONURIA KIT

PKU Enzymatic/Colorimetric - Newborn Phe Screening
Dried blood spot phenylalanine dehydrogenase assay detects >2mg/dL Phe confirming classic PKU (PAH deficiency).

SIZES:

Different Sizes are Available

PKU Kit - Newborn Screening Applications

Phe >4mg/dL prompts immediate dietary restriction preventing IQ loss >30 points and microcephaly.

Neonatal labs process 24-48h Guthrie spots achieving 99.9% sensitivity before neurologic damage Day 7 life.

Distinguishes classic PKU (PAH <1%) vs BH4 deficiency requiring sapropterin therapy.

Positive predictive value >30% prevents unnecessary dietary trials.

Made	Saudi Made
Standards	SFDA, ISO 13485
Product	PKU PHENYLKETONURIA KIT
Cat. No.	11014XXX (Tailored to your needs: The final digits of the product code correspond to your chosen size and concentration.)
Size	Different Sizes are Available
Shelf Life	2 Years

Clinical chemistry

PKU PHENYLKETONURIA KIT

SIZES:

PKU Kit - Newborn Screening Applications

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