Title: Familial Dominant Drusen with Cnvm: A Case Report

Authors: Dr Anusha Pawar, Dr Sonal Bangwal, Dr Piyush Bajaj, Dr Tripti Choudhary

 DOI:  https://dx.doi.org/10.18535/jmscr/v5i8.52

Abstract

Hereditary drusen are an autosomal dominant entity. The most important factor is age-related so-called typical drusen. But this entity is characterized by an early appearance of drusen. The clinical appearance of familial drusen is variable, ranging from a few large, coarse lesions to numerous tiny dots. Because of the possibility of loss of vision in the younger years, an early diagnosis of familial drusen in necessary. No known effective treatment exists for Familial Dominant Drusen. Follow up is required in cases of Familial Dominant Drusen as occurence of CNVM is a possibility. Prompt treatment is required for the same.

KEYWORDS: Familial dominant drusen, choroidalneovascular membrane, malattialeventinese, Doyne honeycomb retinal dystrophy.

References

  1. Kasmann B, Volcker H. Familial drusen of the macula. Fortschr Ophthalmology. 1990;87(6):567-70.
  2. [Internet]. ONE NETWORK. 2017 [cited 1 August 2017]. Available from: http://file:///C:/Users/hp/Desktop/Familial%20(Dominant)%20Drusen.html
  3. Vaclavik V, Munier F. Macular Dystrophies. 2017.
  4. Eye Rounds.org: Malattia Leventinese (Familial Dominant Drusen): 30 year-old female with drusen [Internet]. Webeye.ophth.uiowa.edu. 2017 [cited 1 August 2017]. Available from: http://webeye.ophth.uiowa.edu/eyeforum/cases/48-Malattia-Leventinese-Familial-Dominant-Drusen.htm

Corresponding Author

Dr Anusha Pawar

Se-161 Shastri Nagar, Ghaziabad, Uttar Pradesh India 201002

09953927339, 08383949510, Email: This email address is being protected from spambots. You need JavaScript enabled to view it.