Pathological, histochemical and ultrastructural studies on 3 siblings with GM 1 gangliosidosis type II are reported. These studies support a biochemical defect with profound deficiency of /~-galactosidase which results in widespread accumulation of the GM 1 ganglioside and its asialo derivative in brain and to a lesser extent in viscera, as well as in storage of a keratan sulphate-like mucopolysaccharide. Striking valvular changes in the heart without myocardial involvement were seen in all eases. The histochemical and ultrastructural changes are similar to those seen in GM~ gangliosidosis type I, though less severe. Autosomal recessive inheritance without apparent ethnic predilection seems likely.