نتایج جستجو برای: mucopolysaccharidosis type

تعداد نتایج: 1343233  

2012
R.M. Castilhos D. Blank C.B.O. Netto C.F.M. Souza L.N.T. Fernandes I.V.D. Schwartz R. Giugliani L.B. Jardim

Progressive myelopathies can be secondary to inborn errors of metabolism (IEM) such as mucopolysaccharidosis, mucolipidosis, and adrenomyeloneuropathy. The available scale, Japanese Orthopaedic Association (JOA) score, was validated only for degenerative vertebral diseases. Our objective is to propose and validate a new scale addressing progressive myelopathies and to present validating data fo...

2017
Rossella Parini Federica Deodato Maja Di Rocco Edoardo Lanino Franco Locatelli Chiara Messina Attilio Rovelli Maurizio Scarpa

Mucopolysaccharidosis I-Hurler (MPS I-H) is the most severe form of a metabolic genetic disease caused by mutations of IDUA gene encoding the lysosomal α-L-iduronidase enzyme. MPS I-H is a rare, life-threatening disease, evolving in multisystem morbidity including progressive neurological disease, upper airway obstruction, skeletal deformity and cardiomyopathy. Allogeneic hematopoietic stem cel...

2016
Eric T. Rush

A 14 year old patient with short stature, type I diabetes, and cataracts was referred for evaluation of avascular necrosis of the femoral head. Radiography was suggestive of spondyloepiphyseal dysplasia with decreased bone mineral density for age. Targeted molecular and biochemical testing were normal in this patient. Whole exome sequencing was performed and showed compound heterozygosity for p...

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