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. 2022 May 28;30(8):1065–1078. doi: 10.1016/j.jsps.2022.05.011

Fig. 4.

Fig. 4

Clinical presentation of childhood-onset mitochondrial diseases. Genotypic and phenotypic features of mitochondrial diseases in children. Abbreviations: ASH, Alpers–Huttenlocher syndrome; myopathy sensory ataxia; ANS, Ataxia neuropathy spectrum; CLA, Congenital lactic acidosis. Created with Biorender.com.