Publication:
Metachromatic Leucodystrophy: A Case Report

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorKarki, Subhana
dc.contributor.authorRai, Ganesh Kumar
dc.contributor.authorKafle, Raju
dc.date.accessioned2026-06-02T08:21:42Z
dc.date.available2026-06-02T08:21:42Z
dc.date.issued2011
dc.descriptionSubhana Karki Assistant Professor, Kanti Children's Hospital, Maharajgunj, Kathmandu, and affiliated to National Academy of Medical Sciences, Bir Hospital, Mahabauddha, Kathmandu Ganesh Kumar Rai Associate Professor, Kanti Children's Hospital, Maharajgunj, Kathmandu, and affiliated to National Academy of Medical Sciences, Bir Hospital, Mahabauddha, Kathmandu Raju Kafle Kanti Children's Hospital, Maharajgunj, Kathmandu, and affiliated to National Academy of Medical Sciences, Bir Hospital, Mahabauddha, Kathmandu
dc.description.abstractAbstract: Metachromatic leukodystrophy (MLD) is an autosomal recessive neurodegenerative disorder characterized by deficient activity of the enzyme arylsulfatase-A. Deficiency of this enzyme results in intralysosomal storage of sphingolipid cerebroside 3-sulfates (sulfatides), which are abundant in myelin and neurons. A pathological hallmark of MLD is demyelination and neurodegeneration, causing various and ultimately lethal neurological symptoms. Its frequency is estimated to be 1/40,000 live births. The disease encompasses three clinical subtypes: late infantile (40% of the patients with MLD), juvenile (40%), and adult (20%).
dc.identifierhttps://doi.org/10.3126/jnps.v31i2.4644
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6335
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectMetachromatic Leucodystrophy
dc.titleMetachromatic Leucodystrophy: A Case Report
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage145
oaire.citation.startPage143
relation.isJournalIssueOfPublicatione43eed01-15df-428a-b74c-608eef074322
relation.isJournalIssueOfPublication.latestForDiscoverye43eed01-15df-428a-b74c-608eef074322
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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