Publication:
Thanatophoric Skeletal Dysplasia: A Case Report

creativeworkseries.issnJNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.authorAnjum, Firoz
dc.contributor.authorDaha, Sunil Kumar
dc.contributor.authorSah, Ganesh
dc.date.accessioned2026-08-14T06:12:59Z
dc.date.available2026-08-14T06:12:59Z
dc.date.issued2020
dc.descriptionFiroz Anjum Department of Pediatrics, Patan Academy of Health Sciences, School of Medicine Patan Hospital, Lalitpur, Nepal Sunil Kumar Daha Department of Pediatrics, Patan Academy of Health Sciences, School of Medicine Patan Hospital, Lalitpur, Nepal Ganesh Sah Department of Pediatrics, Patan Academy of Health Sciences, School of Medicine Patan Hospital, Lalitpur, Nepal
dc.description.abstractAbstract Thanatophoric skeletal dysplasia is the most lethal, rare, sporadic birth defect due to de novo mutation in the fibroblast growth factor receptor-3. Clinically this is characterized by shortening of the limbs (micromelia), small conical thorax, flat vertebral bodies and macrocephaly at birth. We encountered a similar case with ultrasonographic findings suggestive of Thanatophoric skeletal dysplasia which resulted into death of the baby within an hour of birth. Almost all cases of this condition have been reported to have died interuterinally or few days after birth. Keywords: birth defect; micromelia; skeletal dysplasia; thanatophoric skeletal dysplasia.
dc.identifierhttps://doi.org/10.31729/jnma.4488
dc.identifier.urihttps://hdl.handle.net/20.500.14572/7297
dc.language.isoen_US
dc.publisherNepal Medical Association
dc.subjectbirth defect
dc.subjectmicromelia
dc.subjectskeletal dysplasia
dc.subjectthanatophoric skeletal dysplasia
dc.titleThanatophoric Skeletal Dysplasia: A Case Report
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage187
oaire.citation.startPage185
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relation.isJournalIssueOfPublication.latestForDiscovery87de1eb3-87c3-4821-8509-4f3fa214619f
relation.isJournalOfPublicatione6e146a0-0ece-4aba-aa0a-6ccfbd10a12a

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