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. Author manuscript; available in PMC: 2023 Nov 1.
Published in final edited form as: Mol Genet Metab. 2022 Sep 19;137(3):230–238. doi: 10.1016/j.ymgme.2022.09.002

Figure 2.

Figure 2.

SNHL occurrence and severity in PMD subjects by genetic subgroup etiology. (A) SNHL frequency and (B) SNHL severity are shown among 193 PMD subjects grouped by genetic etiology. (C) SNHL in PMD subjects with mtDNA gene pathogenic variants. Only mtDNA variants identified in individuals with audiological confirmed SNHL are shown. SNHL, sensorineural hearing loss.; PMD, Primary Mitochondrial Disease; **p-value <0.01; *** p-value <0.001