Fig. 2From: Genetic rhabdomyolysis within the spectrum of the Spinocerebellar Ataxia type 2 responsive to pregabalinCryosections of muscle biopsy showed scattered atrophic, polygonal and angulated myofibers without inflammation, myofiber necrosis or pathologic inclusions (H&E stain, 200x) (a) and myofiber type grouping characteristic of chronic neurogenic atrophy (myosin ATPase activity stain at pH 9.4, 200x) (b).Back to article page