Amanda A. Marques, Sabrina R. Ribeiro, Sabrina de C. Brasil, Flávio R. F. Alves
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C.E. Credit. Kabuki Syndrome and Its Oral Manifestations: A Case Report
Background Kabuki Syndrome is a rare genetic alteration of autosomal origin, known for five characteristics called Niikawa’s Pentad: skeletal abnormalities, short stature, mild to moderate intellectual and developmental disabilities, facial dysmorphism, dermatoglyphic alterations, and postnatal growth deficiency.