A Case of Stickler Syndrome Type I Caused by a Novel Variant of COL2A1 Gene |
Lee, Jin
(Division of Pediatric Endocrinology and Metabolism, Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine)
Jung, Chang-Woo (Division of Pediatric Endocrinology and Metabolism, Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) Kim, Gu-Hwan (Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) Lee, Beom-Hee (Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) Choi, Jin-Ho (Division of Pediatric Endocrinology and Metabolism, Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) Yoo, Han-Wook (Division of Pediatric Endocrinology and Metabolism, Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) |
1 | Baker S, Booth C, Fillman C, Shapiro M, Blair MP, Hyland JC, et al. A loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome. Am J Med Genet A 2011;155A:1668-72. |
2 | Snead MP, Payne SJ, Barton DE, Yates JR, al-Imara L,Pope FM, et al. Stickler syndrome: correlation between vitreoretinal phenotypes and linkage to COL 2A1. Eye 1994;8:609-14. DOI ScienceOn |
3 | Richards AJ, Laidlaw M, Whittaker J, Treacy B, Rai H, Bearcroft P, et al. High efficiency of mutation detection in type 1 stickler syndrome using a two-stage approach: vitreoretinal assessment coupled with exon sequencing for screening COL2A1. Hum Mutat 2006;27:696-704. DOI ScienceOn |
4 | Spranger J, Winterpacht A, Zabel B. The type II collagenopathies: a spectrum of chondrodysplasias. Eur J Pediatr 1994;153:56-65. |
5 | Printzlau A, Andersen M. Pierre Robin sequence in Denmark: a retrospective population-based epidemiological study. Cleft Palate Craniofac J 2004;41:47-52. DOI ScienceOn |
6 | Lee DE, Kim IT. Stickler's syndrome. J Korean Ophthalmol Soc 1996;37:559-63. |
7 | ES L, JA K, GY J, HS C, SH P. A Case of Stickler Syndrome with Large Eyeballs. J Korean Soc Neonatol 1998;5: 242-7. |
8 | YH C, YS S, SY L, HJ P, GS C, BH H. An anesthetic experience in a patient with Stickler sydrome: A case report. Anesth Pain Med 2011;6:85-8. |
9 | Nishimura G, Haga N, Kitoh H, Tanaka Y, Sonoda T, Kitamura M, et al. The phenotypic spectrum of COL2A1 mutations. Hum Mutat 2005;26:36-43. DOI ScienceOn |
10 | Hoornaert KP, Vereecke I, Dewinter C, Rosenberg T, Beemer FA, Leroy JG, et al. Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients. Eur J Hum Genet 2010;18: 872-80. DOI ScienceOn |
11 | Stickler GB, Belau PG, Farrell FJ, Jones JD, Pugh DG,Steinberg AG, et al. Hereditary Progressive Arthro- Ophthalmopathy. Mayo Clin Proc 1965;40:433-55. |
12 | Richards AJ, Yates JR, Williams R, Payne SJ, Pope FM, Scott JD, et al. A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1 (XI) collagen. Hum Mol Genet 1996;5:1339-43. DOI |
13 | Stickler GB, Hughes W, Houchin P. Clinical features of hereditary progressive arthro-ophthalmopathy (Stickler syndrome): a survey. Genet Med 2001;3:192-6. DOI ScienceOn |
14 | Snead MP, Yates JR. Clinical and Molecular genetics of Stickler syndrome. J Med Genet 1999;36:353-9. |
15 | Williams CJ, Ganguly A, Considine E, McCarron S, Prockop DJ, Walsh-Vockley C, et al. A-2-->G transition at the 3' acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original Stickler syndrome kindred. Am J Med Genet 1996;63:461-7. DOI ScienceOn |
16 | Vikkula M, Mariman EC, Lui VC, Zhidkova NI, Tiller GE, Goldring MB, et al. Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus. Cell 1995;80:431-7. DOI ScienceOn |
17 | Van Camp G, Snoeckx RL, Hilgert N, van den Ende J, Fukuoka H, Wagatsuma M, et al. A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene. Am J Hum Genet 2006;79:449-57. DOI ScienceOn |