Fig. 2From: Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 geneH syndrome. a Large, hyperpigmented, and hypertrichotic skin patches involving symmetrically the inner aspects of both thighs and shins. b Multidigit camptodactyly of the handsBack to article page