Galactosialidosis

MONDO:0009737

A lysosomal storage disease characterized by coarse facial features, macular ''cherry red spot'', and dysostosis multiplex. Clinical presentation can be heterogenous ranging from a severe, early-onset, rapidly progressive infantile form to late onset, slowly progressive juvenile/adult form.

Also known as: Goldberg syndrome, galactosialidosis, neuraminidase deficiency with beta-galactosidase deficiency, GSL, PPCA deficiency, cathepsin A deficiency, cathepsin A deficiency of, lysosomal protective Protein deficiency

75 clinical trials for this condition and its sub-types.

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