Publication:
Lissencephaly with Congenital Hypothyroidism: A Case Report

creativeworkseries.issnJNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.authorSahani, Shambhu Kumar
dc.contributor.authorPathak, Anil
dc.contributor.authorNepali, Bishal
dc.contributor.authorRai, Nilshan
dc.date.accessioned2025-11-06T06:44:22Z
dc.date.available2025-11-06T06:44:22Z
dc.date.issued2022
dc.descriptionShambhu Kumar Sahani KIST Medical College and Teaching Hospital, Imadol, Lalitpur, Nepal Anil Pathak KIST Medical College and Teaching Hospital, Imadol, Lalitpur, Nepal. Bishal Nepali KIST Medical College and Teaching Hospital, Imadol, Lalitpur, Nepal Nilshan Rai KIST Medical College and Teaching Hospital, Imadol, Lalitpur, Nepal
dc.description.abstractAbstract Lissencephaly is a malformation of cortical development associated with deficient neuronal migration and abnormal formation of cerebral convolutions or gyri. The lissencephaly spectrum consists of agyria, pachygyria, and subcortical band heterotopia. At least 19 genes have been identified in the causation of lissencephaly and related syndrome. Lissencephaly is associated with many other congenital disorders but the association of lissencephaly with congenital hypothyroidism is rarely reported. We report a case of a 10-year-old girl having lissencephaly with congenital hypothyroidism. Early diagnosis of lissencephaly and genetic counselling can be made in suspected cases and further possible interventions can be taken. Also, regular follow-up, monitoring, and better conservative management lead to a better prognosis.
dc.identifierhttps://doi.org/10.31729/jnma.7893
dc.identifier.urihttps://hdl.handle.net/20.500.14572/3072
dc.language.isoen_US
dc.publisherNepal Medical Association
dc.subjectCongenital abnormalities
dc.subjectHypothyroidism
dc.subjectLissencephaly
dc.subjectNeuronal migration disorders
dc.titleLissencephaly with Congenital Hypothyroidism: A Case Report
dc.typeOther
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage981
oaire.citation.startPage978
relation.isJournalIssueOfPublicatione2f2f036-234f-4302-8cf3-16306564c925
relation.isJournalIssueOfPublication.latestForDiscoverye2f2f036-234f-4302-8cf3-16306564c925
relation.isJournalOfPublicatione6e146a0-0ece-4aba-aa0a-6ccfbd10a12a

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