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Description
LHON Leber hereditary optic neuropathy, MELAS mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes, ADOA autosomal dominant optic atrophy, MNGIE mitochondrial neurogastrointestinal encephalomyopathy, MIDD maternally inherited diabetes and deafness Determining the exact global incidence of mitochondrial diseases is challenging due to their rarity, high mortality, and clinical and genetic heterogeneity

Tratamentul poate fi prelungit conform recomandrii medicului specialist

Independent of the sample volume provided, the ligand is highly specific
Our service uses hydroxocobalamin, the standard Vitamin B12 injection widely used in the UK
When you inject GHK-Cu subcutaneously, the peptide enters circulation and distributes throughout your body

& Keogh, J
