This syndrome associates gingival fibromatosis with dental abnormalities including generalized thin hypoplastic amelogenesis imperfecta, intrapulpal calcifications, and delay of tooth eruption. It has been described in four patients from a consanguineous family. One of the patients presented with intellectual deficit. Transmission is autosomal recessive.
Quelle: Orphanet: an online rare disease and orphan drug data base. Copyright, INSERM 1997. Available on http://www.orpha.net. Accessed 14.04.2014
Gingivahyperplasie, Zahnanomalien, Amelogenesis imperfecta, Dentitio tarda