Alteration of liver enzymes is a feature of the MYH9-related disease syndrome.

PLoS One · 2012 · PMC3338476 · PMID 22558294

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0.0700

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nearly significantp = 0.07so close (0.05 < p ≤ 0.1)

However, when causative mutations were grouped by the involved exon of MYH9 , mutations of exon 25 (T1155I, T1155A, and R1162T) were associated with a higher prevalence of elevation of both aminotrasferases (p = 0.04) and with a higher level of increase of ALT (p = 0.02); a nearly significant association was observed also for a higher elevation of AST (p = 0.07).

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