Other Names for this Disease
- Goldberg syndrome
- Neuraminidase deficiency with beta-galactosidase deficiency
- Lysosomal protective protein deficiency of
- Protective protein/Cathepsin A deficiency
- Cathepsin A deficiency of
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Galactosialidosis is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.
Last updated: 5/16/2011
- Galactosialidosis. Genetics Home Reference (GHR). 2009; http://ghr.nlm.nih.gov/condition/galactosialidosis. Accessed 5/16/2011.