Galactosialidosis is a lysosomal storage disease. This condition is rare and most cases have been in the juvenile/adult group of patients. An infantile form has been described. ==Molecular biology== It is associated with cathepsin A. This disease is due to mutations in the CTSA gene which encodes the protective protein/cathepsin A (PPCA). This in ...
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http://en.wikipedia.org/wiki/Galactosialidosis
(gә-lak″to-si-al″ĭ-do´sis) an autosomal recessive disorder clinically almost identical to sialidosis type II but due to a deficiency of both sialidase and β-galactosidase.
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http://www.encyclo.co.uk/local/21001
galactosialidosis An autosomal recessive disorder clinically almost indistinguishable from sialidosis, type II, but due to deficiency of both sialidase and β-galactosidase. As in sialidosis, multiple variants occur, of increasing severity with decreasing age of onset; congenital, infantile, and juvenile forms have been identified. The defect ...
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http://www.wordinfo.info/words/index/info/view_unit/1954/
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