• Users Online: 182
  • Home
  • Print this page
  • Email this page
Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 
OPHTHA INSTA
Year : 2020  |  Volume : 32  |  Issue : 2  |  Page : 126-127

The mystery of the missing pit


Department of Ophthalmology, Government Medical College, Thrissur, Kerala, India

Correspondence Address:
Dr. Neethu Pradeep
Department of Ophthalmology, Government Medical College, Thrissur, Kerala
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/kjo.kjo_61_20

Rights and Permissions

Foveal hypoplasia refers to the underdevelopment of fovea, characterized by the continuity of the inner retinal layers in the presumed foveal area; the foveal avascular zone may be limited or absent, and retinal vessels may be seen coursing through the foveal region. It is usually associated with aniridia, albinism, achromatopsia, or retinopathy of prematurity. Isolated foveal hypoplasia is a rare clinical entity. We hereby report a case of congenital nystagmus with foveal hypoplasia. Fundus finding in isolated foveal hypoplasia though typical is very subtle and often difficult to detect, especially due to accompanying nystagmus. The presence of nystagmus and poor vision in infants or children without any ocular finding should prompt the ophthalmologist to carry out a thorough fundus examination of the foveal area and to perform an optical coherence tomography to confirm the diagnosis.


[FULL TEXT] [PDF]*
Print this article     Email this article
 Next article
 Previous article
 Table of Contents

 Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
 Citation Manager
 Access Statistics
 Reader Comments
 Email Alert *
 Add to My List *
 * Requires registration (Free)
 

 Article Access Statistics
    Viewed184    
    Printed15    
    Emailed0    
    PDF Downloaded42    
    Comments [Add]    

Recommend this journal