Children's Mitochondrial Disease Network

Mayfield House
30 Heber Walk
Chester Way

Tel (Helpline): 01606 43946 Web:

The Children's Mitochondrial Disease Network is a registered charity in the UK concentrating on the specialities and complexities of Mitochondrial Disorders in children and adults.

The following are Mitochondrial Disorders: Alpers Disease; Barth Syndrome (Cardiomyopathy); Carnitine Deficiency; Kearns-Sayre Syndrome (KSS); Lethal Infantile Mitochondrial Disease (LIMD); Laigh's Disease/Syndrome (LD/LS); Luft Disease; Leber's Hereditary Optic Neuropathy (LHON); Mitochondrial Cytopathy; Mitochondrial Encephalomyopathy; Mitochondrial Myopathy: infant, child & adult onset; Mitochondrial DNA Deletions, Point Mutations & Depletions (mtDNA); Nuclear Encoded DNA Defects (nDNA); Mitochondrial Encephalomyopathy, Lactic Acidosis & Stroke-like Episodes (MELAS); Neuropathy, Ataxia & Retinitis Pigmentosa (NARP); Progressive External Ophthalomglia (PEO); Pearson Marrow Syndrome; Cytochrome C Oxidase Deficiency type A, B, C (COX); Pyruvate Dehydrogenase Deficiency Complex E1 & E2 (PDH); Pyruvate Carboxylase Deficiency (PCH); Phosphoenolpyruvae Carbokinase Deficiency (PEPK); Hypertrophic Cardiomyopathy (HMC); Mitochondrial Fatty Oxidation Disorders (MCAD, MCHAD, SCAD, LCAD, VLACD, CPI & II, ETF, GAII, MADD, HMG; Oxidative Phosporylation Diseases; MENKES Disease; MINGIE Disease.

Last updated on 21/07/2012

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