Literature DB >> 16148630

Early diagnosis of the papillorenal syndrome by optic disc morphology.

Arif O Khan1, Sawsan R Nowilaty.   

Abstract

The morphology of optic disc dysplasia is the most consistent finding in the papillorenal syndrome, an autosomal-dominant syndrome of eye and kidney maldevelopment often associated with the PAX2 mutation. In the absence of a recognized family history, the diagnosis is typically not made until renal disease is evident. We report an infant whose characteristic fundus findings led to the early diagnosis of the papillorenal syndrome before the potential development of renal dysfunction.

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Year:  2005        PMID: 16148630     DOI: 10.1097/01.wno.0000177303.67715.74

Source DB:  PubMed          Journal:  J Neuroophthalmol        ISSN: 1070-8022            Impact factor:   3.042


  3 in total

1.  Papillorenal syndrome-causing missense mutations in PAX2/Pax2 result in hypomorphic alleles in mouse and human.

Authors:  Ramakrishna P Alur; Camasamudram Vijayasarathy; Jacob D Brown; Mohit Mehtani; Ighovie F Onojafe; Yuri V Sergeev; Elangovan Boobalan; Marypat Jones; Ke Tang; Haiquan Liu; Chun-Hong Xia; Xiaohua Gong; Brian P Brooks
Journal:  PLoS Genet       Date:  2010-03-05       Impact factor: 5.917

2.  Three New PAX2 Gene Mutations in Patients with Papillorenal Syndrome.

Authors:  Alberto Galvez-Ruiz; Anthony J Lehner; Alicia Galindo-Ferreiro; Patrik Schatz
Journal:  Neuroophthalmology       Date:  2017-05-08

Review 3.  Cavitary anomalies of the optic disc: neurologic significance.

Authors:  Karl C Golnik
Journal:  Curr Neurol Neurosci Rep       Date:  2008-09       Impact factor: 5.081

  3 in total

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