Hurler Syndrome: A report of three cases.

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dc.contributor.authorMakhela, J
dc.contributor.authorKaushal, K
dc.contributor.authorChoraria, S
dc.contributor.authorRanka, M
dc.contributor.authorPatel, S B
dc.date.accessioned2015-10-23T06:52:57Z
dc.date.available2015-10-23T06:52:57Z
dc.date.issued2015-06
dc.description.abstractThe mucopolysaccharidoses (MPS) are a group of inherited metabolic disorders that result in widespread skeletal, visceral, and mental abnormalities. A defect in metabolic degradation leads to the storage of mucopolysaccharide macromolecules in the nervous system and other body tissues. The MPS are classified into various types, and there are additional diseases, such as the mucolipidoses and a gangliosidosis, that demonstrate similar clinical and radiologic findings. We hereby present 3 cases of Hurler Syndrome, TypeI mucopolysaccharidoses, and enumerate there radiological characteristic radiological findings.en_US
dc.identifier.citationMakhela J, Kaushal K, Choraria S, Ranka M, Patel S B. Hurler Syndrome: A report of three cases. International Archives of Integrated Medicine. 2015 Jun; 2(6): 210-213.en_US
dc.identifier.issn2394-0026 (P)
dc.identifier.issn2394-0034 (O)
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/164756
dc.language.isoenen_US
dc.source.urihttps://iaimjournal.com/wp-content/uploads/2015/06/iaim_2015_0206_27.pdfen_US
dc.titleHurler Syndrome: A report of three cases.en_US
dc.typeArticleen_US
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