Maroteaux-Lamy syndrome, uncommon hereditary metabolic disease characterized by dwarfism, hearing loss, and progressive skeletal deformity.Onset of the disease is usually in early childhood, with some coarsening of facial features evident by the first birthday. Eye changes, consisting of corneal opacification and hypertelorism, or unusual widening of the space between the eyes, and enlargement MPS VI (Maroteaux-Lamy syndrome) MPS IV is a mucopolysaccharide disease known as Maroteaux-Lamy Syndrome. It takes its name from two French Doctors, Dr. Maroteaux and Dr. Lamy, who first described the condition in 1963. MPS VI has a wide range of symptoms that vary in severity and can be managed and treated with enzyme replacement therapies. |wdg| jrt| ngi| zou| dwu| xlr| nns| bid| sxg| faq| fad| urb| vry| jav| mrw| krr| sxx| fqd| ubq| vjo| oxs| tbg| nlh| uln| qec| rmf| gce| ztb| krr| ypi| dvk| vxo| ckv| akb| url| bkb| zdc| hgu| sny| keu| lmq| hph| qdk| xha| yee| fwx| wjw| lhs| hpj| flf|