LEIGH SYNDROME MITOCHONDRIAL MUTATION DETECTION

LEIGH SYNDROME MITOCHONDRIAL MUTATION DETECTION

138 Ratings

Rs 7,205 Rs 5,500

24 % OFF

LEIGH SYNDROME IS A HETEROGENOUS NEUROLOGIC DISORDER DUE TO DAMAGE IN MITOCHONDRIAL ENERGY PRODUCTION THAT USUALLY STARTS IN EARLY CHILDHOOD. THERE IS PROGRESSIVE ENCEPHALOPATHY WITH EPISODIC NEURO-DEGENERATION, ATAXIA, DYSTONIA, NYSTAGMUS AND VISION LOSS. RARELY IT ARISES IN ADULTS.

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4 ML (2 ML MIN.) WHOLE BLOOD IN 1 LAVENDER TOP (EDTA) TUBE. SHIP REFRIGERATED. DO NOT FREEZE. DULY FILLED GENOMICS CLINICAL INFORMATION REQUISITION FORM IS MANDATORY.

PCR, SEQUENCING

REPORT ON 15TH DAY EVENING 7PM

DULY FILLED GENOMICS CLINICAL INFORMATION REQUISITION FORM IS MANDATORY.

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