Shirian S, Shahabinejad H, Saeedzadeh A, Daneshbod K, Khosropanah H, Mortazavi M, Daneshbod Y. Zimmermann-Laband syndrome: Clinical and cytogenetic study in two related patients. J Clin Exp Dent. 2019;11(5):e452-6.

 

doi:10.4317/jced.55214

http://dx.doi.org/10.4317/jced.55214

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References

1. Chadwick B, Hunter B, Hunter L, Aldred M, Wilkie A. Laband syndrome. Report of two cases, review of the literature, and identification of additional manifestations. Oral Surg Oral Med Oral Pathol. 1994:78:57-63.
https://doi.org/10.1016/0030-4220(94)90118-X

 

2. Sattur AP, Burde KN, Nailmasur VG, Goyal M. Zimmermann-Laband syndrome: Report of a Case with early cardiac complications. Journal of Indian Academy of Oral Medicine and Radiology. 2010;22:174-176.
https://doi.org/10.5005/jp-journals-10011-1043

 

3. Castori M, Valiante M, Pascolini G, Leuzzi V, Pizzuti A, Grammatico P. Clinical and genetic study of two patients with ZimmermanneLaband syndrome and literature review. Eur J Med Genet. 2013;56:570-576
https://doi.org/10.1016/j.ejmg.2013.08.004
PMid:23994350

 

4. Crotwell PL, Hoyme HE. Advances in whole-genome genetic testing: from chromosomes to microarrays. Curr Probl Pediatr Adolesc Health Care. 2012;42:47-73.
https://doi.org/10.1016/j.cppeds.2011.10.004
PMid:22325474

 

5. Bartsch O, Schindler D, Beyer V, Gesk S, van't Slot R, Feddersen I, et al. A girl with an atypical form of ataxia telangiectasia and an additional de novo 3.14 Mb microduplication in region19q12. Eur J Med Genet. 2012;55:49-55.
https://doi.org/10.1016/j.ejmg.2011.08.001
PMid:21893220

 

6. Lin, Z., et al., Report of a case of Zimmermann-Laband syndrome with new manifestations. Int J Oral Maxillofac Surg, 2010;39:937-41.
https://doi.org/10.1016/j.ijom.2010.01.023
PMid:20457511

 

7. Kim HG, Higgins AW, Herrick SR, Kishikawa S, Nicholson L, Kutsche K, Ligon AH, Harris DJ, MacDonald ME, Bruns GA, Morton CC, Quade BJ, Gusella JF. Candidate loci for Zimmermann-Laband syndrome at 3p14.3. Am J Med Genet A. 2007;143A:107-11.
https://doi.org/10.1002/ajmg.a.31544
PMid:17163523

 

8. Wynne SE, Aldred MJ, Bartold PM. Hereditary gingival fibromatosis associated with hearing loss and supernumerary teeth--a new syndrome. J Periodontol, 1995;66:75-9.
https://doi.org/10.1902/jop.1995.66.1.75
PMid:7891255

 

9. Stefanova M, Atanassov D, Krastev T, Fuchs S, Kutsche K. Zimmermanne Laband syndrome associated with a balanced reciprocal translocation t(3;8)(p21.2;q24.3) in mother and daughter: molecular cytogenetic characterization of the breakpoint regions. Am J Med Genet. 2003;117A:289-294.
https://doi.org/10.1002/ajmg.a.10174
PMid:12599195

 

10. Hoogendijk CF, Marx J, Honey EM, Pretorius E, Christianson AL. Ultrastructural investigation of Zimmermann-Laband syndrome. Ultrastruct Pathol. 2006;30:423-426.
https://doi.org/10.1080/01913120601042245
PMid:17182434

 

11. Hu P, Wang Y, Meng LL, Qin L, Ma DY, Yi L, et al. 1q25.2-q31.3 Deletion in a female with mental retardation, clinodactyly, minor facial anomalies but no growth retardation. Mol Cytogenet. 2013;6:30.
https://doi.org/10.1186/1755-8166-6-30
PMid:23915434 PMCid:PMC3766032

 

12. Schinzel A. Possible trisomy 1q25 leads to 1q32 in a malformed girl with a de novo insertion in 1q. Hum Genet. 1979;49:167-73.

 

13. Warden CR, Pillers DA, Rice MJ, Wildes J, Livingston JS, Clark BA, et al. Interstitial duplication of the short arm of chromosome 1 in a newborn with congenital heart disease and multiple malformations. Am J Med Genet. 2001;101:100-105.
https://doi.org/10.1002/ajmg.1337
PMid:11391651

 

14. O'Driscoll M, Jeggo P. The role of double-strand break repair e insights from human genetics, Nat Rev Genet 2006;7:45-54.
https://doi.org/10.1038/nrg1746
PMid:16369571

 

15. Couteau F, Zetka M. DNA damage during meiosis induces chromatin remodeling and synaptonemal complex disassembly. Dev Cell 2011;20:353-363.
https://doi.org/10.1016/j.devcel.2011.01.015
PMid:21397846

 

16. Kloosterman WP, Guryev V, van Roosmalen M, Duran KJ, de Bruijn E, Bakker SC, et al. Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline. Hum Mol Genet. 2011;20:1916-1924.
https://doi.org/10.1093/hmg/ddr073
PMid:21349919