Cleidocranial dysplasia: Radiological mimic of pyknodysostosis – A case report

Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disorder with predominant membranous bone involvement. It may also occur as a sporadic mutation. The diagnosis of this condition is based on the clinical, radiological and genetic findings. It is characterised by hypoplasia or aplas...

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Detalles Bibliográficos
Autores principales: Kaur, Harmeet, Gupta, Kamini, Tiwari, Punit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837811/
https://www.ncbi.nlm.nih.gov/pubmed/31754500
http://dx.doi.org/10.4102/sajr.v22i1.1326

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837811/
https://www.ncbi.nlm.nih.gov/pubmed/31754500
http://dx.doi.org/10.4102/sajr.v22i1.1326

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