Oral Surgery Procedures in a Patient with Hajdu-Cheney Syndrome Treated with Denosumab—A Rare Case Report

Background: Hajdu-Cheney syndrome (HCS) is a very rare autosomal-dominant congenital disease associated with mutations in the NOTCH2 gene. This disorder affects the connective tissue and is characterized by severe bone resorption. Hajdu-Cheney syndrome most frequently affects the head and feet bones...

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Detalles Bibliográficos
Autores principales: Kaczoruk-Wieremczuk, Magdalena, Adamska, Paulina, Adamski, Łukasz Jan, Wychowański, Piotr, Jereczek-Fossa, Barbara Alicja, Starzyńska, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8431733/
https://www.ncbi.nlm.nih.gov/pubmed/34501688
http://dx.doi.org/10.3390/ijerph18179099

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8431733/
https://www.ncbi.nlm.nih.gov/pubmed/34501688
http://dx.doi.org/10.3390/ijerph18179099

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