MANNOSIDOSIS
\mˌanəsɪdˈə͡ʊsɪs], \mˌanəsɪdˈəʊsɪs], \m_ˌa_n_ə_s_ɪ_d_ˈəʊ_s_ɪ_s]\
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Inborn error of metabolism marked by a defect in alpha-mannosidase activity that results in lysosomal accumulation of mannose-rich substrates. Virtually all patients have psychomotor retardation, facial coarsening, and some degree of dysostosis multiplex. It is thought to be an autosomal recessive disorder.
By DataStellar Co., Ltd
