Gardner’s syndrome

Ophthalmology Reports ›› 2013, Vol. 6 ›› Issue (1) : 82 -83. DOI: 10.17816/OV2013182-83

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Gardner’s syndrome

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Edward Cherney. Gardner’s syndrome. Ophthalmology Reports, 2013, 6(1): 82-83 DOI:10.17816/OV2013182-83

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[1]	Gardner E.J., Stephens F.E. Cancer of the lower digestive tract in one family group. // Am. J. Hum. Genet. — 1950. — March, Vol. 2 (1). — P. 41–48.

[2]	Gardner E. J., Richards R. C. Multiple cutaneous and subcutaneous lesions occurring simultaneously with hereditary polyposis and osteomatosis. // Am. J. Hum. Genet. — 1953. — Vol. 5. — P. 139–147.

[3]	Fader M., Kline S. N., Spatz S. S., Zubrow H. J. Gardner's syndrome (intestinal polyposis, osteomas, sebaceous cysts) and a new dental discovery. // Oral Surg. Oral Med. Oral Pathol. — 1962. — Feb, Vol. 15. — 153–172.

[4]	Asman H. B. Pierce E. R. Familial polyposis. A statistical study of a large Kentucky kindred Cancer. // 1970, Apr. 25(4). — P. 972–981.

[5]	Gardner E. J., Burt R. W., Freston J. W. Gastro-intestinal polyposis: syndromes and genetic mechanisms. // West. J. Med. — 1980. — Vol. 132. — P. 488–499.

[6]	Blair N. P., Trempe C. L. Hypertrophy of the retinal pigment epithelium associated with Gardner's syndrome. // Am. J. Ophthalmol. — 1980. — Vol. 90. — P. 661–667.

[7]	Lewis R. A., Crowder W. E., Eierman L. A., Nussbaum R. L., Ferrell R. E. The Gardner syndrome: significance of ocular features. // Ophthalmology. — 1984. — Vol. 91. — P. 916–925.

[8]	Shields J. A., Shields C. L., Shah P. G., Pastore D. J. Imperiale SM Jr.: Lack of association amonh typical congenital hypertrophy of the retinal pigment epithelium, adenomatous polyposis and Gardner syndrome. // Ophthalmology. — 1992. — Nov, Vol. 99(11). — P. 1709–1713

[9]	Traboulsi E. I., Murphy S. F., de la Cruz Z. C., Maumenee I. H., Green W. R. A clinicopathologic study of the eyes in familial adenomatous polyposis with extracolonic manifestations (Gardner's syndrome). // Am. J. Ophthalmol. — 1990. — Nov, Vol. 15, 110(5). — P. 550–561.