Abstract
The prevalence and mode of inheritance of major genetic eye diseases have been investigated in China since the establishment of the Section of Ophthalmic Genetics of the Chinese Society of Genetics. Mass screening of genetic eye diseases has been undertaken in many districts in China, covering more than 700,000 people, and more than 5000 pedigrees of genetic eye diseases have been collected and analysed all over China. Based on these data, the prevalence and mode of inheritance of dyschromatopsia, degenerative myopia, retinitis pigmentosa, congenital ptosis, congenital microphthalmos, congenital cataract, congenital glaucoma, Leber's optic atrophy, corneal dystrophy, congenital nystagmus, coloboma of the eye, congenital aniridia, retinoblastoma, macular dystrophy, simple myopia, primary glaucoma, and strabismus have been investigated, and the results are presented.
Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Grizzard W. S., Deutman A. F., Nijhuis F., de Kerk A. A. Crystalline retinopathy. Am J Ophthalmol. 1978 Jul;86(1):81–88. doi: 10.1016/0002-9394(78)90019-3. [DOI] [PubMed] [Google Scholar]
- Hu D. N. Genetic aspects of retinitis pigmentosa in China. Am J Med Genet. 1982 May;12(1):51–56. doi: 10.1002/ajmg.1320120107. [DOI] [PubMed] [Google Scholar]
- Hu D. N. Twin study on myopia. Chin Med J (Engl) 1981 Jan;94(1):51–55. [PubMed] [Google Scholar]
- Smith C. Recurrence risks for multifactorial inheritance. Am J Hum Genet. 1971 Nov;23(6):578–588. [PMC free article] [PubMed] [Google Scholar]