Late-onset retinal macular degeneration: clinical insights into an inherited retinal degeneration (Reprinted from British Journal of Ophthalmology, vol 93, pg 284-9, 2009)

S. Borooah, C. Collins, A. Wright, B. Dhillon

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

Aim: This study describes, in detail, the phenotype of late-onset retinal macular degeneration (L-ORMD) an inherited condition affecting both the retina and anterior segment. A staging based on clinical characteristics is proposed, and the relevance of this condition to current understanding of age-related macular degeneration is discussed.

Methods: A systematic review of the literature regarding this condition supports a detailed description of the natural history. Clinical experiences in identifying, monitoring and managing patients are also presented.

Results: L-ORMD is a rare fully penetrant autosomal dominant condition resulting from a mutation in the C1QTNF5 gene on chromosome 11. Affected individuals develop bilateral loss of vision, dark-adaptation abnormalities, fundus drusen-like yellow spots, midperipheral pigmentation, choroidal neovascularisation, chorioretinal atrophy and long anteriorly inserted lens zonules. Patients may benefit from treatment with high-dose vitamin A.

Conclusions: Raised awareness of L-ORMD should lead to earlier diagnosis and improved care for patients. New antivascular endothelial growth factor treatment may provide a new possibility for management. A deeper insight into molecular and genetic mechanisms of L-ORMD may suggest avenues to explore new treatments of this disorder.

Original languageEnglish
Pages (from-to)495-500
Number of pages6
JournalPostgraduate Medical Journal
Volume85
Issue number1007
DOIs
Publication statusPublished - Sept 2009

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