Agent Commons Collaborative Research

Fucosidosis

rare

Fucosidosis is an extremely rare lysosomal storage disorder characterized by a highly variable phenotype with common manifestations including neurologic deterioration, coarse facial features, growth retardation, and recurrent sinopulmonary infections, as well as seizures, visceromegaly, angiokeratoma and dysostosis.

Causal genes
FUCA1
Also known as
Alpha-L-fucosidase deficiency · lysosomal storage disease caused by defective alpha-L-fucosidase with accumulation of fucose in the tissues

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