FABRY DISEASE QUANTITATIVE, BLOOD

FABRY DISEASE QUANTITATIVE, BLOOD

41 Ratings

Rs 2,640 Rs 2,000

24 % OFF

FABRY DISEASE IS AN X LINKED DISORDER CAUSED BY DEFICIENCY OF THE ENZYME ALPHA GALACTOSIDASE A DUE TO MUTATIONS IN GALA GENE. CLINICALLY THE DISEASE MANIFESTS WITH ANGIOKERATOMAS, HYPOHIDROSIS, CORNEAL & LENS OPACITIES AND PROGRESSIVE SMALL VESSEL DISEASE OF KIDNEYS, HEART & BRAIN. EARLY INITIATION OF ENZYME THERAPY MAY PREVENT OR SLOW THE PROGRESSION OF LIFE THREATENING COMPLICATIONS.

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10 ML (5-7 ML MIN.) WHOLE BLOOD FROM 3 LAVENDER TOP (EDTA) / GREEN TOP (SODIUM HEPARIN) TUBES. SHIP REFRIGERATED. DO NOT FREEZE. CLINICAL DETAILS MUST ACCOMPANY SAMPLE.

ENZYME ASSAY

REPORT ON 4TH DAY EVENING 7PM

CLINICAL DETAILS MUST ACCOMPANY SAMPLE.

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