Doyne honeycomb retinal dystrophy
Other Names for this Disease
- Doyne honeycomb degeneration of retina
drusen that accumulate beneath the retinal pigment epithelium (the pigmented layer of the retina). Over time, drusen may grow and come together, creating a honeycomb pattern. It usually begins in early to mid adulthood, but the age of onset varies. The degree of vision loss also varies. DHRD is usually caused by mutations in the EFEMP1 gene and is inherited in an autosomal dominant manner.Doyne honeycomb retinal dystrophy (DHRD) is a condition that affects the eyes and causes vision loss. It is characterized by small, round, white spots known as
Last updated: 10/20/2014
- Evans K. et al. Assessment of the phenotypic range seen in Doyne honeycomb retinal dystrophy. Arch Ophthalmol. 1997; 115(7):904-910.
- Marla J. F. O'Neill. DOYNE HONEYCOMB RETINAL DYSTROPHY; DHRD. OMIM. December 1, 2009; http://omim.org/entry/126600. Accessed 2/10/2012.
- Doyne Honeycomb Degeneration of the Retina. University of Arizona. 2010; http://disorders.eyes.arizona.edu/category/alternate-names/doyne-honeycomb-degeneration-retina. Accessed 2/10/2012.
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- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Doyne honeycomb retinal dystrophy. Click on the link to view a sample search on this topic.