Gingival fibromatozis sendromları (herediter)
Kalıtsal - AD
Etkilenen kromozomların farklı olduğu 5 fenotip (2'si herediter)
Tüm fenotiplerde tek bulgu: gingival fibromatozis
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Xiao S, Bu L, Zhu L, et al. A new locus for hereditary gingival fibromatosis (GINGF2) maps to 5q13-q22. Genomics, 74: 180-185, 2001
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Hart TC, Zhang Y, Gorry MC, et al. A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1. American Journal of Human Genetics, 70: 943-954, 2002
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Ye X, Shi L, Cheng Y, et al. A novel locus for autosomal dominant hereditary gingival fibromatosis, GINGF3, maps to chromosome 2p22.3-p23.3. Clinical Genetics, 68: 239-244, 2005
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Zhu Y, Zhang W, Huo Z, et al. A novel locus for maternally inherited human gingival fibromatosis at chromosome 11p15 Human Genetics, 121: 113-123, 2007
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Pehlivan D, Abe S, Öztürk S, et al. Cytogenetic analysis and examination of SOS1 gene mutation in a Turkish family with hereditary gingival fibromatosis. Journal of Hard Tissue Biology, 18: 131-134, 2009
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Bayram Y, White JJ, Elçioğlu N, et al. REST final-exon-truncating mutations cause hereditary gingival fibromatosis. American Journal of Human Genetics, 101: 149-156, 2017