Literature DB >> 1634741

Norrie's disease vs. PHPV: one family's dilemma.

F LaRussa1, M D Wesson.   

Abstract

This paper presents the numerous similarities between Norrie's disease and bilateral persistent hyperplastic primary vitreous. A description of each disease is given, as well as a case report which demonstrates the difficulty in distinguishing the two disease processes when there is a negative family history of blindness. A discussion section focuses on the need for a better differential protocol for Norrie's disease, which would aid the clinician when a family history of blindness is absent.

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Year:  1992        PMID: 1634741

Source DB:  PubMed          Journal:  J Am Optom Assoc        ISSN: 0003-0244


  3 in total

1.  Reduced bone mineral density and hyaloid vasculature remnants in a consanguineous recessive FEVR family with a mutation in LRP5.

Authors:  L M Downey; H M Bottomley; E Sheridan; M Ahmed; D F Gilmour; C F Inglehearn; A Reddy; A Agrawal; J Bradbury; C Toomes
Journal:  Br J Ophthalmol       Date:  2006-09       Impact factor: 4.638

2.  Persistent hyperplastic primary vitreous: diagnosis, treatment and results.

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

3.  Bilateral persistent fetal vasculature due to a mutation in the Norrie disease protein gene.

Authors:  Seyedmehdi Payabvash; Jill S Anderson; David R Nascene
Journal:  Neuroradiol J       Date:  2015-10-12
  3 in total

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