A case report of pyknodysostosis with cleidocranial dysplasia: Computed tomography and panoramic imaging

Pyknodysostosis is an extremely rare autosomal recessive genetic osteosclerotic disorder caused by cathepsin K deficiency leading to decrease in the bone turnover. It is characterized by short stature, brachycephaly, short and stubby fingers, open cranial sutures and fontanelle, and diffuse osteoscl...

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Main Authors: Dharmraj Meena (Author), Mohammed Zuber (Author), Samadhan Pawar (Author), Shweta Rani (Author)
Formato: Livro
Publicado em: Wolters Kluwer Medknow Publications, 2013-01-01T00:00:00Z.
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