INCLUSION CELL DISEASES
\ɪnklˈuːʒən sˈɛl dɪzˈiːzɪz], \ɪnklˈuːʒən sˈɛl dɪzˈiːzɪz], \ɪ_n_k_l_ˈuː_ʒ_ə_n s_ˈɛ_l d_ɪ_z_ˈiː_z_ɪ_z]\
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A group of inherited metabolic diseases characterized by the accumulation of excessive amounts of acid mucopolysaccharides, sphingolipids, and/or glycolipids in visceral and mesenchymal cells. Abnormal amounts of sphingolipids or glycolipids are present in neural tissue. Mental retardation and skeletal changes, most notably dysostosis multiplex, occur frequently. (From Joynt, Clinical Neurology, 1992, Ch56, pp36-7)
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