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Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/19204
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dc.contributor.authorAbdul Jalil, Muhammad Fahmi-
dc.contributor.authorRussell, Jeremy-
dc.contributor.authorDelatycki, Martin B-
dc.contributor.authorGonzalvo, Augusto-
dc.date2016-06-
dc.date.accessioned2018-09-13T00:21:11Z-
dc.date.available2018-09-13T00:21:11Z-
dc.date.issued2016-06-
dc.identifier.citationClinical neurology and neurosurgery 2016;145:6-7-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/19204-
dc.description.abstractWe report a man with biparietal foramina secondary to Potocki-Shaffer syndrome. This is due to incomplete ossification of parietal bones secondary to haploinsuffiency of ALX4 gene. He presented with multiple episodes of concussion following minimal head trauma. Cranioplasty was performed to close the skull defects with the aim of preventing further concussion and permanent traumatic brain injury.-
dc.language.isoeng-
dc.subjectBiparietal foramina-
dc.subjectConcussion-
dc.subjectCranioplasty-
dc.subjectPotocki-Shaffer syndrome-
dc.titleCongenital biparietal foramina presenting with multiple concussions.-
dc.typeJournal Article-
dc.identifier.journaltitleClinical neurology and neurosurgery-
dc.identifier.affiliationDepartment of Clinical Genetics, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Neurosurgery, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.doi10.1016/j.clineuro.2016.03.013-
dc.identifier.pubmedid27058439-
dc.type.austinCase Reports-
dc.type.austinJournal Article-
local.name.researcherDelatycki, Martin B
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptClinical Genetics-
crisitem.author.deptNeurosurgery-
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