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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Detalles Bibliográficos
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

Internet

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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