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.
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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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