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See Latest ArticlesCraniometaphyseal dysplasia: A case report
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics, 05/29/09
Lamazza L et al. - The authors present a 36-year-old male with a previous diagnosis of Paget disease. The examination reveals prognathism, ocular hypertelorism, mixed bilateral hypoacusia, nasal bossing, a class III malocclusion and a narrow palatal vault. The histological report led to an exclusion of the previous diagnosis of Paget disease. The final diagnosis of autosomal dominant CMD was confirmed by the molecular testing of the CMD gene (ANKH).
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Assessing for primary oropharyngeal or nasopharyngeal squamous cell carcinoma from fine needle aspiration of cervical lymph node metastases
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The Use of Freeze-Dried Bone Allograft as an Alternative to Autogenous Bone Graft in the Atrophic Maxilla: A 3-Year Clinical Follow-up
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