Literature DB >> 30451201

Persistent fetal vasculature - Clinical spectrum.

Aditi Mehta1, Simar Rajan Singh1, Mohit Dogra1, Jagat Ram1.   

Abstract

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Year:  2018        PMID: 30451201      PMCID: PMC6256874          DOI: 10.4103/ijo.IJO_1042_18

Source DB:  PubMed          Journal:  Indian J Ophthalmol        ISSN: 0301-4738            Impact factor:   1.848


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Persistent fetal vasculature (PFV) is a congenital anomaly caused due to incomplete regression of the hyaloidal fetal vasculature.[123] Fig. 1a shows a Mitterndorf dot – a circular opacity on the posterior lens capsule, nasal to the center, which represents the anterior attachment of the hyaloid artery. Fig. 1b shows limited anterior PFV obscuring the visual axis with a classical stalk. Fig. 1c demonstrates PFV presenting with a vascularized membrane and prominent ciliary processes. Fig. 1d images the remnant posterior end of the stalk, the Bergmeister papilla. Identification of these clinical signs enables correct diagnosis and management of PFV.
Figure 1

Clinical spectrum of Persistent Fetal Vasculature (PFV). (a) Mitterndorf dot. (b) Limited anterior PFV with stalk. (c) PFV with a vascularized membrane and prominent ciliary processes. (d) Bergmeister papilla

Clinical spectrum of Persistent Fetal Vasculature (PFV). (a) Mitterndorf dot. (b) Limited anterior PFV with stalk. (c) PFV with a vascularized membrane and prominent ciliary processes. (d) Bergmeister papilla

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  3 in total

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Authors:  M F Goldberg
Journal:  Am J Ophthalmol       Date:  1997-11       Impact factor: 5.258

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Authors:  Z F Pollard
Journal:  Trans Am Ophthalmol Soc       Date:  1997

3.  Outcomes of cataract surgery in children with persistent hyperplastic primary vitreous.

Authors:  Jitender Jinagal; Parul C Gupta; Jagat Ram; Manu Sharma; Simar R Singh; Sonam Yangzes; Jaspreet Sukhija; Ramandeep Singh
Journal:  Eur J Ophthalmol       Date:  2017-09-14       Impact factor: 2.597

  3 in total

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