Cerebral and occipito-atlanto-axial involvement in mucopolysaccharidosis patients: clinical, radiological, and neurosurgical features

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lysosomal storage disease 1 endocrinologydiseases
mucopolysaccharidosis 3 endocrinologydiseases

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Select Drug Character Offset Drug Term Instance
Select Disease Character Offset Disease Term Instance
lysosomal storage disease 3119 eligible for surgery.BackgroundMucopolysaccharidoses (MPS) are a group of inherited autosomal recessive lysosomal storage disease s (except for MPS II, which is sex-linked) caused by the deficiency of the enzymes involved in the degradation
mucopolysaccharidosis 87 Title: Italian Journal of PediatricsCerebral and occipito-atlanto-axial involvement in mucopolysaccharidosis patients: clinical, radiological, and neurosurgical featuresCarlo GiussaniLelio GuidaFrancesco CanonicoErik
mucopolysaccharidosis 380 (pmc-release): 11/2018Publication date (collection): /2018AbstractBackgroundNeurosurgical features of mucopolysaccharidosis (MPS) patients mainly involve the presence of cranio-vertebral junction (CVJ) abnormalities and the
mucopolysaccharidosis 4554 occurrence rate of hydrocephalus/ventriculomegaly, brain atrophy, and spinal stenosis in patients with mucopolysaccharidosis (MPS)Hydrocephalus/ventriculomegalyAtrophySpinal stenosisMPS I Hurler+++++++ Hurler/Scheie+++++ Scheie++++++MPS

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