Modified Le Fort I Osteotomy and Genioplasty for Management of Severe Dentofacial Deformity in β-Thalassaemia Major: Case report and review of the literature

β-thalassaemia major is an autosomal recessive form of haemoglobinopathy that is characterised by complete lack of production of the β-chains resulting in multiple complications that include severe anaemia, failure to thrive and skeletal abnormalities. Facial deformities induced by β-thalassaemia ma...

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Detalles Bibliográficos
Autores principales: Al Hasani, Khamis M., Bakathir, Abdulaziz A., Al-Hashmi, Ahmed K., Al Rawahi, Badar, Albakri, Abdullah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sultan Qaboos University Medical Journal, College of Medicine & Health Sciences 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7574809/
https://www.ncbi.nlm.nih.gov/pubmed/33110654
http://dx.doi.org/10.18295/squmj.2020.20.03.018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7574809/
https://www.ncbi.nlm.nih.gov/pubmed/33110654
http://dx.doi.org/10.18295/squmj.2020.20.03.018

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