Gingival fibromatozis sendromları (herediter)

Kalıtsal - AD

Etkilenen kromozomların farklı olduğu 5 fenotip (2'si herediter)

Tüm fenotiplerde tek bulgu: gingival fibromatozis

 

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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