This stromal dystrophy may be congenital as it can be seen in the first years of life.  It is nonprogressive and generally has little clinical significance as it does not impair vision or require treatment in most cases.  It is usually diagnosed on routine examination from the presence of multiple, minute, whitish or grayish discrete opacities throughout the stroma.  The largest numbers are located centrally and posteriorly.  These may be flat, round or oval, and sometimes resemble snowflakes.  Keratocyte cell bodies contain cytoplasmic inclusions or vacuoles likely as the result of defective intracellular organelle trafficking.  Other layers such as the epithelium, Bowman layer, Descemet and endothelium are normal.  Expressivity is highly variable with considerable asymmetry of opacities in the two eyes and even unilateral involvement.