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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Galactosialidosis


Other Names for this Disease

  • Cathepsin A deficiency of
  • Goldberg syndrome
  • GSL
  • Lysosomal protective protein deficiency of
  • Neuraminidase deficiency with beta-galactosidase deficiency
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Inheritance

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How is galactosialidosis inherited?

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.[1]
Last updated: 5/16/2011

References
  1. Galactosialidosis. Genetics Home Reference (GHR). 2009; http://ghr.nlm.nih.gov/condition/galactosialidosis. Accessed 5/16/2011.


Other Names for this Disease
  • Cathepsin A deficiency of
  • Goldberg syndrome
  • GSL
  • Lysosomal protective protein deficiency of
  • Neuraminidase deficiency with beta-galactosidase deficiency
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.