MUCOLIPIDOSIS TYPE IV
\mjˌuːkəlˌɪpɪdˈə͡ʊsɪs tˈa͡ɪp ɹˌə͡ʊmən fˈɔː], \mjˌuːkəlˌɪpɪdˈəʊsɪs tˈaɪp ɹˌəʊmən fˈɔː], \m_j_ˌuː_k_ə_l_ˌɪ_p_ɪ_d_ˈəʊ_s_ɪ_s t_ˈaɪ_p ɹ_ˌəʊ_m_ə_n_ f_ˈɔː]\
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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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