| mannosidosis |
a lysosomal storage disease due to defective α-mannosidase with resultant oligosaccharide accumulation. Characteristics include coarse facies, upper respiratory congestion and infections, profound mental retardation, hepatosplenomegaly, cataracts, radiographic signs of dysostosis multiplex, and kyphosis. Mannosidosis is divided into type I (infantile onset) and type II (juvenile-adult onset).
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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