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Lessons from a case of osteopetrosis oxycephaly and Chiari type I malformation: a case report
We report a child with osteopetrosis, oxycephaly and Chiari type I malformation who presented with raised intracranial pressure. During cranial expansion surgery the patient developed sudden cardiac arrest which we believe was probably related to the Chiari malformation. The case highlights a previo...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Cases Network Ltd
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2740010/ https://www.ncbi.nlm.nih.gov/pubmed/19829859 http://dx.doi.org/10.4076/1757-1626-2-6787 |
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author | Jamjoom, Aimun AB Jamjoom, Bakur A Waliuddin, Abrar R Jamjoom, Abdulhakim B |
author_facet | Jamjoom, Aimun AB Jamjoom, Bakur A Waliuddin, Abrar R Jamjoom, Abdulhakim B |
author_sort | Jamjoom, Aimun AB |
collection | PubMed |
description | We report a child with osteopetrosis, oxycephaly and Chiari type I malformation who presented with raised intracranial pressure. During cranial expansion surgery the patient developed sudden cardiac arrest which we believe was probably related to the Chiari malformation. The case highlights a previously unrecognized association between osteopetrosis, craniosynostosis and a persistently open fontanelle at age 4 years. In addition it supports the existing literature in emphasizing the need for careful preoperative work up, choice of approach and operative technique in children with complex craniosynostosis and Chiari malformation. |
format | Text |
id | pubmed-2740010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Cases Network Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-27400102009-10-14 Lessons from a case of osteopetrosis oxycephaly and Chiari type I malformation: a case report Jamjoom, Aimun AB Jamjoom, Bakur A Waliuddin, Abrar R Jamjoom, Abdulhakim B Cases J Case report We report a child with osteopetrosis, oxycephaly and Chiari type I malformation who presented with raised intracranial pressure. During cranial expansion surgery the patient developed sudden cardiac arrest which we believe was probably related to the Chiari malformation. The case highlights a previously unrecognized association between osteopetrosis, craniosynostosis and a persistently open fontanelle at age 4 years. In addition it supports the existing literature in emphasizing the need for careful preoperative work up, choice of approach and operative technique in children with complex craniosynostosis and Chiari malformation. Cases Network Ltd 2009-07-27 /pmc/articles/PMC2740010/ /pubmed/19829859 http://dx.doi.org/10.4076/1757-1626-2-6787 Text en © 2009 Jamjoom et al.; licensee Cases Network Ltd. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case report Jamjoom, Aimun AB Jamjoom, Bakur A Waliuddin, Abrar R Jamjoom, Abdulhakim B Lessons from a case of osteopetrosis oxycephaly and Chiari type I malformation: a case report |
title | Lessons from a case of osteopetrosis oxycephaly and Chiari type I malformation: a case report |
title_full | Lessons from a case of osteopetrosis oxycephaly and Chiari type I malformation: a case report |
title_fullStr | Lessons from a case of osteopetrosis oxycephaly and Chiari type I malformation: a case report |
title_full_unstemmed | Lessons from a case of osteopetrosis oxycephaly and Chiari type I malformation: a case report |
title_short | Lessons from a case of osteopetrosis oxycephaly and Chiari type I malformation: a case report |
title_sort | lessons from a case of osteopetrosis oxycephaly and chiari type i malformation: a case report |
topic | Case report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2740010/ https://www.ncbi.nlm.nih.gov/pubmed/19829859 http://dx.doi.org/10.4076/1757-1626-2-6787 |
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