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Congenital cataracts and their molecular genetics

期刊

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
卷 19, 期 2, 页码 134-149

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2007.10.003

关键词

lens; cataract; molecular genetics; gene

资金

  1. Intramural NIH HHS [Z01 EY000272-17] Funding Source: Medline
  2. NATIONAL EYE INSTITUTE [Z01EY000281, Z01EY000272] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Cataract can be defined as any opacity of the crystalline lens. Congenital cataract is particularly serious because it has the potential for inhibiting visual development, resulting in permanent blindness. Inherited cataracts represent a major contribution to congenital cataracts, especially in developed countries. While cataract represents a common end stage of mutations in a potentially large number of genes acting through varied mechanisms in practice most inherited cataracts have been associated with a subgroup of genes encoding proteins of particular importance for the maintenance of lens transparency and homeostasis. The increasing availability of more detailed information about these proteins and their functions and is making it possible to understand the pathophysiology of cataracts and the biology of the lens in general. Published by Elsevier Ltd.

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