Publication:
Morquio disease with CNS involvement: a rare association

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorPal, Shinabi
dc.contributor.authorDey, Chandrashekhar
dc.contributor.authorGhosh, Nilanjan
dc.contributor.authorRoy, Shabarna
dc.contributor.authorNayek, Kaustav
dc.contributor.authorDasgupta, Malay Kumar
dc.date.accessioned2026-03-30T09:03:55Z
dc.date.available2026-03-30T09:03:55Z
dc.date.issued2014
dc.descriptionShinabi Pal MBBS, MD, Post Graduate Trainee, Department of Paediatrics, RG Kar Medical College, Kolkata Chandrashekhar Dey MBBS, MD, Post Graduate Trainee, Department of Paediatrics, RG Kar Medical College, Kolkata Nilanjan Ghosh MBBS, RMO cum Clinical Tutor, Department of Paediatrics, RG Kar Medical College, Kolkata Shabarna Roy MBBS, RMO Cum Clinical Tutor, Paeditrics, Department of Paediatrics, RG Kar Medical College, Kolkata Kaustav Nayek Professor of Paediatrics, Department of Paediatrics, RG Kar Medical College, Kolkata Malay Kumar Dasgupta MBBS, MD, Professor of Paediatrics, Department of Paediatrics, RG Kar Medical College, Kolkata
dc.description.abstractAbstract: Morquio syndrome is a rare type of mucopolysaccharidosis. Our patient presented with uncontrolled seizures and gross skeletal deformity. He was suspected to be suffering from mucopolysaccharidosis based on his disease presentation but the diagnosis could be made as Morquio syndrome on the basis of the presence of keratan sulphate in the urine.
dc.identifierhttps://doi.org/10.3126/jnps.v34i2.9298
dc.identifier.urihttps://hdl.handle.net/20.500.14572/5536
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectMorquio disease
dc.subjectmucopolysaccharidosis(MPS)
dc.subjectglycosaminoglycans
dc.titleMorquio disease with CNS involvement: a rare association
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage159
oaire.citation.startPage157
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relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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