MUCOPOLYSACCHARIDOSIS II
\mjuːkˈɒpəlˌɪsɐkˌɑːɹɪdˈə͡ʊsɪs ɹˌə͡ʊmən tˈuː], \mjuːkˈɒpəlˌɪsɐkˌɑːɹɪdˈəʊsɪs ɹˌəʊmən tˈuː], \m_j_uː_k_ˈɒ_p_ə_l_ˌɪ_s_ɐ_k_ˌɑː_ɹ_ɪ_d_ˈəʊ_s_ɪ_s ɹ_ˌəʊ_m_ə_n_ t_ˈuː]\
Sort: Oldest first
-
Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15.
By DataStellar Co., Ltd
Word of the day
basidiomycota
- comprises fungi bearing the spores on basidium: Gasteromycetes (puffballs); Tiliomycetes (comprising orders Ustilaginales (smuts) and Uredinales (rusts)); Hymenomycetes (mushrooms; toadstools; agarics; bracket fungi); in some classification systems considered a division of kingdom comprises fungi bearing spores on a basidium; includes Gasteromycetes (puffballs) Tiliomycetes comprising the orders Ustilaginales (smuts) and Uredinales (rusts) Hymenomycetes (mushrooms, toadstools, agarics bracket fungi).