About OJO | Search | Ahead of print | Current Issue | Archives | Author Instructions | Reviewer Guidelines | Online submissionLogin 
Oman Journal of Ophthalmology Oman Journal of Ophthalmology
  Editorial Board | Subscribe | Advertise | Contact
https://www.omanophthalmicsociety.org/ Users Online: 664  Wide layoutNarrow layoutFull screen layout Home Print this page  Email this page Small font size Default font size Increase font size


 
 Table of Contents    
CLINICAL IMAGE
Year : 2017  |  Volume : 10  |  Issue : 1  |  Page : 50-51  

Lipemia retinalis in 1-month-old infant


Department of Pediatric Retina and Ocular Oncology, Aravind Eye Hospital and Postgraduate Institute of Ophthalmology, Coimbatore,Tamil Nadu, India

Date of Web Publication21-Feb-2017

Correspondence Address:
Parag K Shah
Department of Pediatric Retina and Ocular Oncology, Aravind Eye Hospital and Postgraduate Institute of Ophthalmology, Avinashi Road, Coimbatore - 641 014, Tamil Nadu
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0974-620X.200698

Rights and Permissions
   Abstract 

We present a rare case of lipemia retinalis secondary to familial lipase deficiency.

Keywords: Familial lipase deficiency, lipemia retinalis, newborn infant


How to cite this article:
Jain NC, Vanteri J, Shah PK, Narendran V. Lipemia retinalis in 1-month-old infant. Oman J Ophthalmol 2017;10:50-1

How to cite this URL:
Jain NC, Vanteri J, Shah PK, Narendran V. Lipemia retinalis in 1-month-old infant. Oman J Ophthalmol [serial online] 2017 [cited 2023 Mar 27];10:50-1. Available from: https://www.ojoonline.org/text.asp?2017/10/1/50/200698


   Introduction Top


Lipemia retinalis is an asymptomatic condition usually not affecting visual acuity. It is most commonly seen in familial hyperchylomicronemia.[1] Rarely can also be due to secondary hyperlipidemia following diabetes or acquired hypercholesterolemia.[2] It usually presents when the triglyceride (TG) levels exceed 2500 mg/dl.[1]


   Case Presentation Top


A 1-month-old female child referred from a private hospital as a diagnosed case of metabolic syndrome for ophthalmic evaluation. There was a history of umbilical discharge on day 27 after birth and her total serum cholesterol was 7000 mg/dl and serum TGs were 8530 mg/dl. Child was born to parents with second-degree consanguineous marriage.

On ocular examination, anterior segment of both eyes was within normal limits. Posterior segment revealed small yellowish optic discs, salmon pink retina, and dilated tortuous milky white retinal blood vessels [Figure 1]. She was diagnosed to have lipemia retinalis secondary to familial lipoprotein lipase (LPL) deficiency. Child was switched to low-fat skimmed milk and advised to come after 1 month. However, she passed away secondary to systemic complications.
Figure 1: Fundus photos of the right and left eye (a and b) showing salmon pink retina (white arrows) and milky white retinal blood vessels (black arrows) suggestive of lipemia retinalis

Click here to view



   Discussion Top


Ocular features associated with hypertriglyceridemia are corneal arcus, corneal opacification, lipemic aqueous, and xanthelasma. Lipemia retinalis usually does not affect vision, but there have been reports of reduced electroretinography waves.[3] However, there have been reports of branch retinal occlusions in adults.[4]

LPL is the rate-limiting enzyme for hydrolysis of TGs in chylomicrons and very low-density lipoproteins. For full enzymatic activity, the presence of apolipoprotein CII is required as a cofactor. The LPL gene is located on chromosome 8p22 and as a result of mutations in this gene, the enzyme is either not produced or becomes catalytically inactive.[1] Patients have increased risk of pancreatitis and they present with hepatosplenomegaly, lipemia retinalis, and eruptive xanthomas. Recurrent pancreatitis ultimately causes pancreatic insufficiency, which is the major threat.[1] Lipid-lowering drugs are not very effective. Increased risk of coronary artery disease is seen in heterozygous carriers as they have decreased high-density lipoproteins. Mainstay of treatment is lifestyle modification which includes strict adherence to fat restriction for life and regular exercise. To decrease risk of pancreatitis, the aim is to maintain TG values <2000 mg/dL.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Zahavi A, Snir M, Kella YR. Lipemia retinalis: Case report and review of the literature. J AAPOS 2013;17:110-1.  Back to cited text no. 1
    
2.
Park YH, Lee YC. Images in clinical medicine. Lipemia retinalis associated with secondary hyperlipidemia. N Engl J Med 2007;357:e11.  Back to cited text no. 2
    
3.
Lu CK, Chen SJ, Niu DM, Tsai CC, Lee FL, Hsu WM. Electrophysiological changes in lipaemia retinalis. Am J Ophthalmol 2005;139:1142-5.  Back to cited text no. 3
    
4.
Nagra PK, Ho AC, Dugan JD Jr. Lipemia retinalis associated with branch retinal vein occlusion. Am J Ophthalmol 2003;135:539-42.  Back to cited text no. 4
    


    Figures

  [Figure 1]



 

Top
   
 
  Search
 
  
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
   Introduction
   Case Presentation
   Discussion
    References
    Article Figures

 Article Access Statistics
    Viewed4163    
    Printed49    
    Emailed0    
    PDF Downloaded132    
    Comments [Add]    

Recommend this journal