Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/75896
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dc.contributor.authorChirakan Charoenvichaen_US
dc.contributor.authorKrit Khwanngernen_US
dc.contributor.authorWimon Sirimaharajen_US
dc.date.accessioned2022-10-16T07:03:31Z-
dc.date.available2022-10-16T07:03:31Z-
dc.date.issued2022-07-01en_US
dc.identifier.issn15363708en_US
dc.identifier.issn01487043en_US
dc.identifier.other2-s2.0-85133101843en_US
dc.identifier.other10.1097/SAP.0000000000003224en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85133101843&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/75896-
dc.description.abstractFrontoethmoidal encephalomeningocele (FEEM) is a rare congenital craniofacial malformation with increased incidence in Southeast Asia, especially in Thailand. Because of its rarity, main treatment obstacles include the lack of surgical treatment techniques and long-term postoperative follow-up data. The authors present the case of a 9-month-old boy who was born with a large isolated nasoorbital type of FEEM, which had a pressure effect on his right eye, nose, and facial complex. Preoperative computed tomography of the facial bone was performed to evaluate the external bony defect. This study aims to present surgical correction of FEEM with Chula's technique and long-term 7-year postoperative follow-up including both clinical and imaging aspects.en_US
dc.subjectMedicineen_US
dc.titleLarge Isolated Nasoorbital Type of Frontoethmoidal Encephalomeningocele : A Case Report with Long-Term Follow-upen_US
dc.typeJournalen_US
article.title.sourcetitleAnnals of Plastic Surgeryen_US
article.volume89en_US
article.stream.affiliationsFaculty of Medicine, Chiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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