Congenital unilateral fibrosis, blepharoptosis, and enophthalmos syndrome

Authors

  • Alex CW Wong Hong Kong Eye Hospital, Department of Ophthalmology & Visual Sciences, The Chinese University of Hong Kong, Kowloon, Hong Kong
  • Dorothy SP Fan Hong Kong Eye Hospital, Department of Ophthalmology & Visual Sciences, The Chinese University of Hong Kong, Kowloon, Hong Kong
  • Hunter KL Yuen Hong Kong Eye Hospital, Department of Ophthalmology & Visual Sciences, The Chinese University of Hong Kong, Kowloon, Hong Kong

Abstract

Congenital fibrosis syndrome is a rare disorder as- sociated with restricted ocular movements, ptosis, and enophthalmos. Imaging may assist in ruling out orbital bony deformity and other pathology in surrounding structures. This report describes the use of combined positron-emission tomography/computed tomography scan to assist with the diagnosis and management of a patient with congenital fibrosis syndrome.

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Published

2009-12-01

How to Cite

1.
Wong AC, Fan DS, Yuen HK. Congenital unilateral fibrosis, blepharoptosis, and enophthalmos syndrome. Hong Kong J Ophthalmol [Internet]. 2009Dec.1 [cited 2024Apr.20];13(1):24-6. Available from: https://hkjo.hk/index.php/hkjo/article/view/55

Issue

Vol. 13 No. 1 (2009)

Section

Case Report

License

The Journal has a fully Open Access policy and publishes all articles under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) licence. For any use other than that permitted by this license, written permission must be obtained from the Journal.

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