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M0032
ME (Mitochondrial Encephalopathy): Mitochondrial Diseases
Test Details: Mitochondrial encephalomyopathy is a condition that affects many of the body's systems, particularly the brain and nervous system (encephalo-) and muscles (myopathy). The signs and symptoms of this disorder most often appear in childhood following a period of normal development, although they can begin at any age. Early symptoms may include muscle weakness and pain, recurrent headaches, loss of appetite, vomiting and seizures.
Category
Molecular Genetics
Pre-test Information
Clinical and family history is mandatory.
Report Delivery
4 working days
Gender
All
Organ
Multi-Organ
ME (Mitochondrial Encephalopathy): Mitochondrial Diseases
4400
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