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Abstract Retinitis pigmentosa (RP) is a group of inherited diseases characterized by primary rod photoreceptor dysfunction and progressive cone cell death. Due to their very high energy demand, the degeneration of photoreceptors may be linked to insufficient energy supply or metabolic imbalance.
Introduction Glaucoma is the second leading cause of blindness worldwide (Quigley, 1996; Quigley and Broman, 2006; Tham et al., 2014). It describes a heterogeneous disorder. Excavation (cupping) of the optic nerve head (ONH) and progressive loss of retinal ganglion cell (RGC) axons are characteristic for glaucoma disease.
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