Abstract
Stickler's syndrome is a congenital disease of connective tissue with considerable ocular and non-ocular lesions. This study reports 12 pedigrees (10 families and two isolated cases) and evaluates some peculiar ocular aspects not previously reported in the syndrome.
Full text
PDFImages in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BURIAN H. M., ALLEN L. Histologic study of the chamber angel of patients with Marfan's syndrome. A discussion of the cases of Theobald, Reeh and Lehman, and Sadi de Buen and Velazquez. Arch Ophthalmol. 1961 Mar;65:323–333. doi: 10.1001/archopht.1961.01840020325003. [DOI] [PubMed] [Google Scholar]
- BURIAN H. M., VON NOORDEN G. K., PONSETI I. V. Chamber angle anomalies in systemic connective tissue disorders. Arch Ophthalmol. 1960 Nov;64:671–680. doi: 10.1001/archopht.1960.01840010673008. [DOI] [PubMed] [Google Scholar]
- Cotlier E., Reinglass H. Marfan-like syndrome with lens involvement. Hyaloideoretinal degeneration with anterior chamber angle, facial, dental, and skeletal anomalies. Arch Ophthalmol. 1975 Feb;93(2):93–106. doi: 10.1001/archopht.1975.01010020099001. [DOI] [PubMed] [Google Scholar]
- Criswick V. G., Schepens C. L. Familial exudative vitreoretinopathy. Am J Ophthalmol. 1969 Oct;68(4):578–594. doi: 10.1016/0002-9394(69)91237-9. [DOI] [PubMed] [Google Scholar]
- Herrmann J., France T. D., Spranger J. W., Opitz J. M., Wiffler C. The Stickler syndrome (hereditary arthroophthalmopathy). Birth Defects Orig Artic Ser. 1975;11(2):76–103. [PubMed] [Google Scholar]
- Knobloch W. H. Inherited hyaloideoretinopathy and skeletal dysplasia. Trans Am Ophthalmol Soc. 1975;73:417–451. [PMC free article] [PubMed] [Google Scholar]
- Liberfarb R. M., Hirose T. The Wagner-Stickler syndrome. Birth Defects Orig Artic Ser. 1982;18(6):525–538. [PubMed] [Google Scholar]
- Nielsen C. E. Stickler's syndrome. Acta Ophthalmol (Copenh) 1981 Apr;59(2):286–295. doi: 10.1111/j.1755-3768.1981.tb02991.x. [DOI] [PubMed] [Google Scholar]
- Regenbogen L., Godel V. Hereditary vitreoretinal degeneration, cleft lip and palate, deafness, and skeletal dysplasia. Am J Ophthalmol. 1980 Mar;89(3):414–418. doi: 10.1016/0002-9394(80)90013-6. [DOI] [PubMed] [Google Scholar]
- STICKLER G. B., BELAU P. G., FARRELL F. J., JONES J. D., PUGH D. G., STEINBERG A. G., WARD L. E. HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY. Mayo Clin Proc. 1965 Jun;40:433–455. [PubMed] [Google Scholar]
- Weingeist T. A., Hermsen V., Hanson J. W., Bumsted R. M., Weinstein S. L., Olin W. H. Ocular and systemic manifestations of Stickler's syndrome: a preliminary report. Birth Defects Orig Artic Ser. 1982;18(6):539–560. [PubMed] [Google Scholar]