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Novel mutation in the COL11A1 gene causing Marshall-Stickler syndrome in three generations of a Bulgarian family Cover

Novel mutation in the COL11A1 gene causing Marshall-Stickler syndrome in three generations of a Bulgarian family

Open Access
|Jul 2021

References

  1. Vallat M, Fritsch D, van Coppenolle F, Detre J, Moze M, Rasbourdin FI. Le syndrome de Stickler ou arthroophtalmopathie progressive héréditaire (Stickler’s syndrome or hereditary progressive arthro-opthalmopathy) [French]. J Fr Ophtalmol. 1985; 8(4): 301307. PMID: 4020040.
  2. Stickler GB, Belau PG, Farrell FJ, Jones JD, Pugh DG, Steinberg AG, et al. Hereditary progressive arthro-ophthalmopathy. Mayo Clin Proc. 1965; 40: 433-455.
  3. Herrmann J, France TD, Spranger JW, Opitz JM, Wiffler C. The Stickler syndrome (hereditary arthroophthalmopathy). Birth Defects Orig Arctic Ser. 1975; 11(2): 76-103.
  4. Marshall D. Ectodermal dysplasia; report of kindred with ocular abnormalities and hearing defect. Am J Ophthalmol. 1958; 45(4 Pt 2): 143-156.
  5. Shanske AL, Bogdanow A, Shprintzen RJ, Marion RW. The Marshall syndrome: Report of a new family and review of literature. Am J Med Genet. 1997; 70(1): 52-57.
  6. Winter RM, Baraitser M, Laurence KM, Donna D, Hall CM. The Weissenbacher-Zweymüller, Stickler, and Marshall Syndromes: Further evidence of their identity. Am J Med Genet. 1983; 16(2): 189-199.
  7. Cohen MM Jr. Letter: The demise of the Marshall syndrome. J Pediatr. 1974; 85(6): 878.
  8. Stratton RF, Lee B, Ramirez F. Marshall syndrome. Am J Med Genet. 1991; 41(1): 35-38.
  9. Aymé S, Preus M. The Marshall and Stickler syndromes: Objective rejection of lumping. J Med Genet. 1984; 21(1): 34-81.
  10. Vintiner GM, Temple IK, Middleton-Price HR, Baraitser M, Malcolm S. Genetic and clinical heterogeneity of Stickler syndrome. Am J Med Genet. 1991; 41(1): 44-48.
  11. Akawi NA, Al Gazali L, Ali BR. Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations. Clin Genet. 2011; 82(2): 147-156.
  12. Majava M, Hoornaert KP, Bartholdi D, Bouma MC, Bouman K, Carrera M, et al. A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype-phenotype correlations in type XI collagenopathies. Am J Med Genet A. 2007; 143A(3): 258-264.
Language: English
Page range: 95 - 98
Published on: Jul 27, 2021
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 2021 M Mladenova, T Todorov, L Grozdanova, V Mitev, A Todorova, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.