Literature DB >> 23504283

Unilateral persistent fetal vasculature coexisting with anterior segment dysgenesis.

Sudarshan Khokhar1, Shikha Gupta, Tarun Arora, Varun Gogia, Tanuj Dada.   

Abstract

Persistent fetal vasculature (PFV) is a common congenital developmental anomaly of the eye which results from failure of the embryological primary vitreous and hyaloid vasculature to regress by the time of birth (Int Ophthalmol Clin 48: 53-62, 2008). Typically, it is divided into anterior, posterior or combined types and is characterized by the presence of a vascular stalk located between the optic disc and the posterior lens capsule (Int Ophthalmol Clin 48: 53-62, 2008). Although it has been reported to manifest itself differently, in our case it presented in a microphthalmic eye as anterior segment dysgenesis with broad-based mid-peripheral synechiae, posterior embryotoxon, iridoschisis, ectropion uveae, hypotony and subluxated cataractous lens with a taut anterior hyaloid face which are rare associations with PFV.

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Mesh:

Year:  2013        PMID: 23504283     DOI: 10.1007/s10792-013-9757-z

Source DB:  PubMed          Journal:  Int Ophthalmol        ISSN: 0165-5701            Impact factor:   2.031


  5 in total

1.  Digenic inheritance of mutations in FOXC1 and PITX2 : correlating transcription factor function and Axenfeld-Rieger disease severity.

Authors:  Daniel Kelberman; Lily Islam; Susan E Holder; Thomas S Jacques; Patrick Calvas; Raoul C Hennekam; Ken K Nischal; Jane C Sowden
Journal:  Hum Mutat       Date:  2011-09-08       Impact factor: 4.878

Review 2.  The vitreo-retinal manifestations of persistent hyperplasic primary vitreous (PHPV) and their management.

Authors:  Olga Cerón; Peter L Lou; Arnold J Kroll; David S Walton
Journal:  Int Ophthalmol Clin       Date:  2008

3.  Approach to cataract with persistent hyperplastic primary vitreous.

Authors:  Sudarshan Khokhar; Lalit Kumar Tejwani; Gaurav Kumar; Rakhi Kushmesh
Journal:  J Cataract Refract Surg       Date:  2011-08       Impact factor: 3.351

4.  [Four cases of persistent hyperplastic primary vitreous].

Authors:  K Yamada; H Ozeki; M Ieda; S Shirai; A Majima
Journal:  Nippon Ganka Gakkai Zasshi       Date:  1997-10

5.  Case of chromosome 6p25 terminal deletion associated with Axenfeld-Rieger syndrome and persistent hyperplastic primary vitreous.

Authors:  Katsuhiro Suzuki; Makoto Nakamura; Emi Amano; Kumiko Mokuno; Shoichiro Shirai; Hiroko Terasaki
Journal:  Am J Med Genet A       Date:  2006-03-01       Impact factor: 2.802

  5 in total

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