Literature DB >> 11030072

Visual loss as the presenting sign of Jeune syndrome.

I Casteels1, E Demandt, E Legius.   

Abstract

We describe a 5-year-old girl with Jeune syndrome. The presenting symptoms included visual loss and night blindness only. In the neonatal period she had surgery on both hands for bilateral polydactyly. Following clinical and radiological examination a diagnosis of Jeune syndrome was proposed. Although Jeune syndrome is often characterized by multiple organ abnormalities, our patient presented with ocular symptoms at the age of 5 years.

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Year:  2000        PMID: 11030072     DOI: 10.1053/ejpn.2000.0313

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  6 in total

1.  The intraflagellar transport protein ift80 is essential for photoreceptor survival in a zebrafish model of jeune asphyxiating thoracic dystrophy.

Authors:  Leah M Hudak; Shannon Lunt; Chi-Hsuan Chang; Ethan Winkler; Halley Flammer; Michael Lindsey; Brian D Perkins
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-03-05       Impact factor: 4.799

2.  Jeune Syndrome.

Authors:  P L Prasad; A N Prasad
Journal:  Med J Armed Forces India       Date:  2011-07-21

3.  Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans.

Authors:  Jan Halbritter; Albane A Bizet; Miriam Schmidts; Jonathan D Porath; Daniela A Braun; Heon Yung Gee; Aideen M McInerney-Leo; Pauline Krug; Emilie Filhol; Erica E Davis; Rannar Airik; Peter G Czarnecki; Anna M Lehman; Peter Trnka; Patrick Nitschké; Christine Bole-Feysot; Markus Schueler; Bertrand Knebelmann; Stéphane Burtey; Attila J Szabó; Kálmán Tory; Paul J Leo; Brooke Gardiner; Fiona A McKenzie; Andreas Zankl; Matthew A Brown; Jane L Hartley; Eamonn R Maher; Chunmei Li; Michel R Leroux; Peter J Scambler; Shing H Zhan; Steven J Jones; Hülya Kayserili; Beyhan Tuysuz; Khemchand N Moorani; Alexandru Constantinescu; Ian D Krantz; Bernard S Kaplan; Jagesh V Shah; Toby W Hurd; Dan Doherty; Nicholas Katsanis; Emma L Duncan; Edgar A Otto; Philip L Beales; Hannah M Mitchison; Sophie Saunier; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2013-10-17       Impact factor: 11.025

4.  Jeune syndrome: description of 13 cases and a proposal for follow-up protocol.

Authors:  J de Vries; J L Yntema; C E van Die; N Crama; E A M Cornelissen; B C J Hamel
Journal:  Eur J Pediatr       Date:  2009-05-10       Impact factor: 3.183

5.  Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins.

Authors:  Rivka A Rachel; Tiansen Li; Anand Swaroop
Journal:  Cilia       Date:  2012-12-03

6.  Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome.

Authors:  Ivan Duran; S Paige Taylor; Wenjuan Zhang; Jorge Martin; Kimberly N Forlenza; Rhonda P Spiro; Deborah A Nickerson; Michael Bamshad; Daniel H Cohn; Deborah Krakow
Journal:  Sci Rep       Date:  2016-09-26       Impact factor: 4.379

  6 in total

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