What syndrome is this? Gingival fibromatosis-hypertrichosis syndrome.
Gingival fibromatosis with hypertrichosis syndrome: Case series of rare syndrome.
Congenital marked hypertrichosis and Laband syndrome in a child: overlap between the gingival fibromatosis-hypertrichosis and Laband syndromes.
Zimmermann-Laband syndrome-associated hereditary gingival fibromatosis.
Kshirsagar JT, Dharani K, Thangavel P.
J Indian Soc Periodontol. 2023 Nov-Dec;27(6):645-650. doi: 10.4103/jisp.jisp_582_22. Epub 2024 Jan 24.
Gingival fibromatosis with congenital hypertrichosis.
Saxena S, Bhatia G, Krishna KM, Mehrotra S.
J Indian Soc Periodontol. 2020 Jan-Feb;24(1):80-82. doi: 10.4103/jisp.jisp_26_19. Epub 2019 Oct 4.
A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management.
Elhossini RM, Sayed IM, Hellal US, Mahmoud SAM, Aglan MS, Hassib NF, Abdel-Hamid MS.
Am J Med Genet A. 2024 Jan;194(1):39-45. doi: 10.1002/ajmg.a.63415. Epub 2023 Sep 26.
Gingival fibromatosis with hypertrichosis syndrome: Case series of rare syndrome.
Balaji P, Balaji SM.
Indian J Dent Res. 2017 Jul-Aug;28(4):457-460. doi: 10.4103/ijdr.IJDR_367_17.
Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis.
Kularbkaew T, Thongmak T, Sandeth P, Daroontum T, Durward CS, Vittayakittipong P, Duke P, Iamaroon A, Kintarak S, Intachai W, Ngamphiw C, Tongsima S, Jatooratthawichot P, Cox TC, Ketudat Cairns JR, Kantaputra P.
Int J Mol Sci. 2024 Aug 15;25(16):8867. doi: 10.3390/ijms25168867.
Syndromes with gingival fibromatosis: A systematic review.
Costa CRR, Braz SV, de Toledo IP, Martelli-Júnior H, Mazzeu JF, Guerra ENS, Coletta RD, Acevedo AC.
Oral Dis. 2021 May;27(4):881-893. doi: 10.1111/odi.13369. Epub 2020 May 25.
Enamel Renal Syndrome: A Systematic Review.
Farias MLM, Ornela GO, de Andrade RS, Martelli DRB, Dias VO, Júnior HM.
Indian J Nephrol. 2021 Jan-Feb;31(1):1-8. doi: 10.4103/ijn.IJN_27_19. Epub 2021 Jan 27.
Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes.
Gao X, Dai P, Yuan YY.
Hum Genet. 2022 Apr;141(3-4):821-838. doi: 10.1007/s00439-021-02310-2. Epub 2021 Jul 7.
Expanding the phenotype of gingival fibromatosis-mental retardation-hypertrichosis (Zimmermann-Laband) syndrome.
Chacon-Camacho OF, Vázquez J, Zenteno JC.
Am J Med Genet A. 2011 Jul;155A(7):1716-20. doi: 10.1002/ajmg.a.34030. Epub 2011 May 27.
Current concepts on gingival fibromatosis-related syndromes.
Poulopoulos A, Kittas D, Sarigelou A.
J Investig Clin Dent. 2011 Aug;2(3):156-61. doi: 10.1111/j.2041-1626.2011.00054.x. Epub 2011 Mar 15.
