RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164061556 T1 Amelogenesis Imperfecta (AI) T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164061556 RD 2024/10/11 AB Inherited condition that affects the enamel of the teeth, making them soft and thin. The teeth are easily damaged and appear discolored because the dentin is visible through the thin enamel.