Publication:
Progeroid Syndrome of De Barsy With Hypocalcemic Seizures

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorCheriathu, J
dc.contributor.authorD'souza, IE
dc.contributor.authorJohn, LJ
dc.contributor.authorBahtimi, R El
dc.date.accessioned2026-05-27T07:36:25Z
dc.date.available2026-05-27T07:36:25Z
dc.date.issued2012
dc.descriptionJ Cheriathu Department of Pediatrics, Gulf Medical College Hospital, Ajman IE D'souza Department of Pediatrics, Gulf Medical College Hospital, Ajman LJ John Department of Pharmacology, Gulf Medical University, Ajman R El Bahtimi Consultant Dermatopathologist, American Hospital, Dubai
dc.description.abstractAbstract: De Barsy et al first reported a rare cutaneo-oculo-cerebral malformation-syndrome now commonly referred as ‘progerioid syndrome of de Barsy’. It is the constellation of progeria-like appearance, cutis laxa, intrauterine growth retardation, corneal clouding and hypotonia. We report a case of Debarsy syndrome in a neonate presented at birth with typical clinical features with hypocalcemic seizures. There are no previous reports among Afghani origin and also first case reported from United Arab Emirates, there have been no reported cases of hypocalcemic seizures.
dc.identifierhttps://doi.org/10.3126/jnps.v32i2.5993
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6268
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectDe Barsy
dc.subjectProgeroid syndrome
dc.subjectcutis laxa
dc.titleProgeroid Syndrome of De Barsy With Hypocalcemic Seizures
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage177
oaire.citation.startPage175
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relation.isJournalIssueOfPublication.latestForDiscoverybee5f04f-02d7-4ebc-9b32-c948670b0393
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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