نتایج جستجو برای: mucopolysaccharidosis type

تعداد نتایج: 1343233  

Journal: :Journal of Inborn Errors of Metabolism and Screening 2018

Journal: :Human mutation 2011
Francesca Bertola Mirella Filocamo Giorgio Casati Matthew Mort Camillo Rosano Anna Tylki-Szymanska Beyhan Tüysüz Orazio Gabrielli Serena Grossi Maurizio Scarpa Giancarlo Parenti Daniela Antuzzi Jaime Dalmau Maja Di Rocco Carlo Dionisi Vici Ilyas Okur Jordi Rosell Attilio Rovelli Francesca Furlan Miriam Rigoldi Andrea Biondi David N Cooper Rossella Parini

Mutational analysis of the IDUA gene was performed in a cohort of 102 European patients with mucopolysaccharidosis type I. A total of 54 distinct mutant IDUA alleles were identified, 34 of which were novel including 12 missense mutations, 2 nonsense mutations, 12 splicing mutations, 5 micro-deletions, 1 micro-duplication 1 translational initiation site mutation, and 1 'no-stop' change (p.X654Re...

Journal: :Archives of disease in childhood 1990
R M John D Hunter R H Swanton

Cardiac involvement is well recognised in most forms of the mucopolysaccharidoses but there is poor documentation of abnormalities specific to Morquio's syndrome (type IV mucopolysaccharidosis). Ten patients with the classic form or type A Morquio's syndrome with a median age of 12.5 years underwent echocardiographic assessment. Abnormalities were detected in six (60%) cases with mitral valve i...

Journal: :Genetics and molecular research : GMR 2007
R P El Dib G M Pastores

Mucopolysaccharidoses are a group of inherited metabolic diseases caused by the absence or deficiency of the lysosomal enzymes that are needed for breaking down glycosaminoglycans (GAGs). Over time, GAGs collect in cells, blood and connective tissues, and increased amounts are excreted in the urine. The result is permanent and includes progressive cell damage that affects the individual's appea...

2017
Sathish Muthukumar Ramalingam Daya Srinivasan Sandhya ArunKumar Joe Louis ChiriyanKandath Sriram Kaliamoorthy

Morquio syndrome or MPS IVA is a rare type of lysosomal storage disease associated with highly specific dental abnormalities. We present two siblings with enamel hypoplasia and skeletal abnormalities. A diagnosis of mucopolysaccharidosis type IVA was reached based on the clinical, radiographic, and dental findings of the patients. The dental findings are useful diagnostic aid for the early diag...

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