Osteopetrosis and Chiari type I malformation: a rare association

Osteopetrosis (OP) is hereditary X-linked, autosomal recessive (ARO), or autosomal dominant (ADO) skeletal disease. ARO has two subtypes, which are infantile malignant and intermediate type. ARO and X-linked OP have poor clinical outcome. ADO is called adult benign type because of the normal life ex...

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Autores principales: Ekici, Mehmet Ali, Cıkla, Ulaş, Bauer, Andrew, Başkaya, Mustafa K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620537/
https://www.ncbi.nlm.nih.gov/pubmed/26503583
http://dx.doi.org/10.1093/jscr/rjv084
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author Ekici, Mehmet Ali
Cıkla, Ulaş
Bauer, Andrew
Başkaya, Mustafa K.
author_facet Ekici, Mehmet Ali
Cıkla, Ulaş
Bauer, Andrew
Başkaya, Mustafa K.
author_sort Ekici, Mehmet Ali
collection PubMed
description Osteopetrosis (OP) is hereditary X-linked, autosomal recessive (ARO), or autosomal dominant (ADO) skeletal disease. ARO has two subtypes, which are infantile malignant and intermediate type. ARO and X-linked OP have poor clinical outcome. ADO is called adult benign type because of the normal life expectancy, which has type I and type II. Here, the authors present an ADO patient with Chiari type I. Concomitant ADO with Chiari type I malformation is an extremely rare condition. Literature research yielded only one case report to date.
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spelling pubmed-46205372015-10-27 Osteopetrosis and Chiari type I malformation: a rare association Ekici, Mehmet Ali Cıkla, Ulaş Bauer, Andrew Başkaya, Mustafa K. J Surg Case Rep Case Reports Osteopetrosis (OP) is hereditary X-linked, autosomal recessive (ARO), or autosomal dominant (ADO) skeletal disease. ARO has two subtypes, which are infantile malignant and intermediate type. ARO and X-linked OP have poor clinical outcome. ADO is called adult benign type because of the normal life expectancy, which has type I and type II. Here, the authors present an ADO patient with Chiari type I. Concomitant ADO with Chiari type I malformation is an extremely rare condition. Literature research yielded only one case report to date. Oxford University Press 2015-10-26 /pmc/articles/PMC4620537/ /pubmed/26503583 http://dx.doi.org/10.1093/jscr/rjv084 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author 2015. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Reports
Ekici, Mehmet Ali
Cıkla, Ulaş
Bauer, Andrew
Başkaya, Mustafa K.
Osteopetrosis and Chiari type I malformation: a rare association
title Osteopetrosis and Chiari type I malformation: a rare association
title_full Osteopetrosis and Chiari type I malformation: a rare association
title_fullStr Osteopetrosis and Chiari type I malformation: a rare association
title_full_unstemmed Osteopetrosis and Chiari type I malformation: a rare association
title_short Osteopetrosis and Chiari type I malformation: a rare association
title_sort osteopetrosis and chiari type i malformation: a rare association
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620537/
https://www.ncbi.nlm.nih.gov/pubmed/26503583
http://dx.doi.org/10.1093/jscr/rjv084
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AT baskayamustafak osteopetrosisandchiaritypeimalformationarareassociation

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