Publication:
Apert Syndrome (Acrocephalosyndactyly): A Rare Syndromic Craniosynostosis

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorShrestha, Mahesh
dc.contributor.authorAdhikari, Neelam
dc.contributor.authorShah, Ganesh
dc.date.accessioned2026-06-15T10:23:00Z
dc.date.available2026-06-15T10:23:00Z
dc.date.issued2009
dc.descriptionMahesh Shrestha Resident MD Paediatrics, National Academy of Medical Sciences, Bir Hospital Neelam Adhikari Chief, Department of Paediatrics, Patan Hospital Ganesh Shah Senior Paediatrician, Patan Hospital. Kathmandu
dc.description.abstractAbstract: We report a premature infant who had multisutural craniosynostosis with pointed head, syndactyly of 2nd, 3rd and 4th fingers of all four limbs and other findings that were consistent with Apert syndrome. This is perhaps the first case of Apert Syndrome reported from Nepal.
dc.identifierhttps://doi.org/10.3126/jnps.v29i2.2046
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6516
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectApert syndrome
dc.subjectcraniosynostosis
dc.subjectsyndactyly
dc.titleApert Syndrome (Acrocephalosyndactyly): A Rare Syndromic Craniosynostosis
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
relation.isJournalIssueOfPublication25edd4c9-3340-4afd-822b-67c22e3fd40a
relation.isJournalIssueOfPublication.latestForDiscovery25edd4c9-3340-4afd-822b-67c22e3fd40a
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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