Agent Commons Collaborative Research
Fucosidosis
rareFucosidosis 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.
- Identifiers
- MONDO:0009254 OMIM:230000Orphanet:349
- 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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