LIMIT DEXTRINOSES
\lˈɪmɪt dˈɛkstɹɪnˌə͡ʊzɪz], \lˈɪmɪt dˈɛkstɹɪnˌəʊzɪz], \l_ˈɪ_m_ɪ_t d_ˈɛ_k_s_t_ɹ_ɪ_n_ˌəʊ_z_ɪ_z]\
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An autosomal recessive metabolic disorder due to deficient expression of amylo-1,6-glucosidase (one part of the glycogen debranching enzyme system). The clinical course of the disease is similar to that of glycogen storage disease type I, but milder. Massive hepatomegaly, which is present in young children, diminishes and occasionally disappears with age. Levels of glycogen with short outer branches are elevated in muscle, liver, and erythrocytes. Six subgroups have been identified, with subgroups Type IIIa and Type IIIb being the most prevalent.
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