Publication:
Hurler Syndrome

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorRao, Kalipatnam Seshagiri
dc.contributor.authorAdhikari, Sudhir
dc.contributor.authorSingh,Sandeep
dc.contributor.authorPoudel, Shankar
dc.contributor.authorBasnet, Sahisnuta
dc.contributor.authorBishwakarma, Ganesh
dc.date.accessioned2026-02-23T09:21:09Z
dc.date.available2026-02-23T09:21:09Z
dc.date.issued2016
dc.descriptionKalipatnam Seshagiri Rao Professor and head of Paediatrics, Manipal Teaching Hospital, Manipal College of Medical Sciences, Pokhara Sudhir Adhikari Assistant Professor, Department of Paediatrics, Manipal Teaching Hospital, Manipal College of Medical Sciences, Pokhara Sandeep Singh Lecturer, Noble Medical College, Biratnagar Shankar Poudel Lecturer, Gandaki Medical College, Pokhara Sahisnuta Basnet Assistant Professor, Department of Paediatrics, Manipal Teaching Hospital, Manipal College of Medical Sciences, Pokhara Ganesh Bishwakarma Lecturer, Department of Paediatrics, Manipal Teaching Hospital, Manipal College of Medical Sciences, Pokhara
dc.description.abstractAbstract: We report a case of Hurler syndrome in 10 years old boy diagnosed on the basis of classical clinical and radiological features. Early diagnosis, genetic counseling and regular follow up with recent modalities of treatment can decrease mortality significantly and the child may grow normally.
dc.identifierhttps://doi.org/10.3126/jnps.v36i3.16349
dc.identifier.urihttps://hdl.handle.net/20.500.14572/4873
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectHurler
dc.subjectα-L-iduronidase
dc.subjectLorinidase
dc.titleHurler Syndrome
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage297
oaire.citation.startPage295
relation.isJournalIssueOfPublication0692fd39-d464-4878-b0ff-743d5b445183
relation.isJournalIssueOfPublication.latestForDiscovery0692fd39-d464-4878-b0ff-743d5b445183
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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