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- W2337308674 abstract "SUMMARY Morquio’s Syndrome is a rare skeletal dysplasia with an autosomal recessive trait inheritance that has characterized with disorder of mucopoly saccharide metabolism. The deficiency of N-acetylgalactosamine-6-sulfate sulphatase cause Type A form, and beta galactosidase deficiency cause Type B form. Dental defects are rarely seen in association with the syndrome. A fourteen year-old female with ugrquio syndrome diagnosis was referred to the clinic of Gazi University Faculty of Dentistry Department of Paediatric Dentistry for function and esthetic problems. These prob lems was treated and consultated with ortodontics. Patient was followed up." @default.
- W2337308674 created "2016-06-24" @default.
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- W2337308674 date "2010-01-01" @default.
- W2337308674 modified "2023-09-27" @default.
- W2337308674 title "MUCOPOLYSACCHARIDOSIS TYPE-IVA ( MORQUIO'S SYNDROME)" @default.
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