PHENYLALANINE NEWBORN SCREEN
340 Ratings
Rs 338 Rs 250
26 % OFF
PHENYLKETONURIA (PKU) IS THE MOST COMMON AUTOSOMAL RECESSIVE INHERITED DISORDER OF AMINO ACID METABOLISM CAUSED BY DEFICIENCY OF ENZYME PHENYLALANINE HYDROXYLASE. THIS ASSAY IS USEFUL FOR EVALUATING PATIENTS WITH HYPERPHENYLALANINEMIA AND MONITORING EFFECTIVENESS OF DIETARY THERAPY.
Why book with us?
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Free and On Schedule Sample Collection
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24/7 Service
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Affordable
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Quick and Accurate Reports
1 DROP OF HEEL PRICK BLOOD EACH ON 3 SPOTS OF FILTER PAPER AVAILABLE FROM TRUEMEDIX. SHIP REFRIGERATED OR FROZEN. CLINICAL DETAILS AND DRUG HISTORY MUST ACCOMPANY SAMPLE.
FLUOROIMMUNOASSAY
REPORT ON 4TH DAY EVENING 7PM
CLINICAL DETAILS AND DRUG HISTORY MUST ACCOMPANY SAMPLE.
