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Orthodontic findings and treatment need in patients with amelogenesis imperfecta: a descriptive analysis

Abstract Introduction : Amelogenesis imperfecta (AI) is a genetically determined, non-syndromic enamel dysplasia that may manifest as hypoplasia, hypomaturation, or hypocalcification and can commonly be classified into four primary groups. In this retrospective analysis, specific orofacial character...

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Autors principals: Stephan Christian Möhlhenrich, Sachin Chhatwani, Peter Schmidt, Kristian Kniha, Jan Postberg, Andreas G. Schulte, Jochen Jackowski, Stefan Zimmer, Gholamreza Danesh
Format: Artigo
Idioma:Inglês
Publicat: BMC 2024-06-01
Col·lecció:Head & Face Medicine
Accés en línia:https://doi.org/10.1186/s13005-024-00436-y
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