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Full-mouth rehabilitation choices depending on amelogenesis imperfecta's type: A familial case report
Salomé Mascarell1,2, Hélène Citterio1,2, Victor Martiano1,2
1AP-HP Groupe Hospitalier Pitié-Salpêtrière Charles Foix Paris France.
Clinical Case Reports
|April 15, 2022
Abstract:
Amelogenesis imperfecta, a rare disease, represents inherited, congenital defects that primarily affect enamel with esthetic and functional impairment affecting everyday life. We present oral rehabilitation of a mother and her son, respectively, suffering from an hypoplastic and an hypocalcified form of AI.

