Global Mitochondrial Myopathies Market Size, Share, Forecast Report, 2020-2027

Mitochondrial myopathy is an umbrella term for rare genetic diseases caused due to defective mitochondria in cells which results in inability of the mitochondria to consume normal levels of oxygen and produce energy. The disease manifests itself from infancy to adulthood.

The market driving factors for global mitochondrial myopathy market are the growing number of cases that are detected, rising number of screening for genetic diseases, incentives provided by governments for rare genetic diseases etc. The market restraints are the poor number of treatment options due to rare nature of the disease, absence of curative treatment etc.

Considering all these factors the market for mitochondrial myopathies is expected to reach $ 600 million by the end of 2023, this market is projected to growing at a CAGR of ~ 3.2 % during 2017-2023.
Segments:

The global mitochondrial myopathies market is segmented on the basis of type and therapies. Based on type, the market has been segmented as Kearns-Sayre syndrome (KSS), Leigh syndrome, Mitochondrial DNA depletion syndrome (MDS), Mitochondrial encephalomyopathy, Mitochondrial neuro-gastrointestinal encephalomyopathy (MNGIE), Myoclonus epilepsy with ragged red fibers (MERRF), Neuropathy, ataxia and retinitis pigmentosa (NARP), Pearson syndrome, Progressive external ophthalmoplegia (PEO). Based on the therapies, the market has been segmented as dietary, supportive, vitamins, coenzymes and antioxidants and other.
Key players of Global Mitochondrial myopathies Market:

Key players profiled in the report are Reata Pharmaceuticals, Inc., Stealth BioTherapeutics, Raptor Pharmaceutical Corp., GeneDx, NeuroVive Pharmaceutical AB, and others.