Literature DB >> 20587883

Senior-Loken syndrome in an Iranian family.

Jamshid Roozbeh1, Maryam Sharifian, Hamid Hosseini, Mohammad Mahdi Sagheb, Saeed Behzadi, Ghanbar Ali Raeisjalali, Alireza Iraniparast, Raha Afshariani, Masume Tohidi, Mostafa Sharifian.   

Abstract

Senior-Loken syndrome is a rare entity that combines familial juvenile nephronophthisis with retinal dystrophy. Herein, we report Senior-Loken syndrome in six members of an Iranian family with progressive blindness and renal failure since childhood. Although, this syndrome was reported from other parts of the world, report of six members of one family with this syndrome is rare. To the best of our knowledge, this is the first report from Iran.

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Mesh:

Year:  2010        PMID: 20587883

Source DB:  PubMed          Journal:  Saudi J Kidney Dis Transpl        ISSN: 1319-2442


  3 in total

1.  Gene mutation analysis in Iranian children with nephronophthisis: a two-center study.

Authors:  Alaleh Gheissari; Maryam Harandavar; Friedhelm Hildebrandt; Daniela A Braun; Maryam Sedghi; Nastaran Parsi; Alireza Merrikhi; Yahya Madihi; Farzaneh Aghamohammadi
Journal:  Iran J Kidney Dis       Date:  2015-03       Impact factor: 0.892

2.  Senior Loken Syndrome.

Authors:  Amarpreet Kaur; Shashi Kant Dhir; Geetika Goyal; Naveen Mittal; R K Goyal
Journal:  J Clin Diagn Res       Date:  2016-11-01

3.  Senior-Loken syndrome secondary to NPHP5/IQCB1 mutation in an Iranian family.

Authors:  Alireza Haghighi; Mohamed Al-Hamed; Safa Al-Hissi; Ann-Marie Hynes; Maryam Sharifian; Jamshid Roozbeh; Nasrollah Saleh-Gohari; John A Sayer
Journal:  NDT Plus       Date:  2011-08-18
  3 in total

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