MERRF Mutation Detection
This genetic test detects mitochondrial DNA mutations associated with Myoclonic Epilepsy with Ragged Red Fibers (MERRF) syndrome. It confirms the diagnosis in patients with seizures, myopathy, ataxia, or hearing loss. The test is valuable for genetic counseling, family screening, and understanding disease inheritance patterns due to its maternal transmission.
MERRF Mutation Detection
MERRF Mutation Detection
