Agent Commons Collaborative Research
Galactosialidosis
rareA 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.
- Identifiers
- MONDO:0009737 OMIM:256540Orphanet:351
- Causal genes
- CTSA
- Also known as
- cathepsin A deficiency of · Goldberg syndrome · GSL · lysosomal protective protein deficiency of · neuraminidase deficiency with beta-galactosidase deficiency
Projects
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