Acta Scientific Ophthalmology (ASOP)
Clinical Image Volume 3 Issue 6
Sumit Kumar*, Lagan Paul, Shalin Shah, Manisha Agarwal and Aditi Singal
Vitreo-Retina, Dr Shroff Charity Eye Hospital, New Delhi, India
*Corresponding Author: Sumit Kumar, Consultant, Vitreo-Retina Department, Dr Shroff Charity Eye Hospital, New Delhi, India.
Received: April 20, 2020; Published: June 01, 2020
A 36 year female presented with bilateral Familial Dominant drusen (Doyne Honeycomb drusen) with active choroidal neovascularization membrane (CNVM) in right eye and scarred CNVM in left eye.
Keywords: Familial Dominant Drusen; Doyne Honeycomb Drusen; CNVM; OCTA; OCT
References
- Pearce WG. “Doyne's honeycomb retinal degeneration. Clinical and genetic features”. British Journal of Ophthalmology 2 (1968): 73-78.
- Vogt A. Handbuch der gesammten Augenheilkunde. Untersuchungsmethoden. 3. Berlin: Springer Verlag (1925).
- Heon E., et al. “Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21”. Archives of Ophthalmology (Chicago, Ill: 1960)2 (1996): 193-198.
- Haimovici R., et al. “Symptomatic abnormalities of dark adaptation in patients with EFEMP1 retinal dystrophy (Malattia Leventinese/Doyne honeycomb retinal dystrophy)”. Eye (London, England)1 (2002): 7-15.
- Anusha Pawar., et al. “Familial Dominant Drusen with Cnvm: A Case Report”. Journal of Medical Science and Clinical Research 8 (2017):26300-26302.
- Pager CK., et al. “Malattia leventinese presenting with subretinal neovascular membrane and hemorrhage”. American Journal of Ophthalmology 4 (2001): 517-518.
- Michael Ehrlich. “Wills Eye Resident Case Series”. Review of Ophthalmology (2017).
Citation
Citation: Sumit Kumar., et al. “Bilateral Choroidal Neovascularization in Doyne Honeycomb Drusen”. Acta Scientific Ophthalmology 3.6 (2020): 36-38.
Copyright
Copyright: © 2020 Sumit Kumar., et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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