Literature DB >> 25584255

Senior- loken syndrome - a ciliopathy.

Hemachandar R1.   

Abstract

Senior - Loken syndrome is a rare combination of juvenile nephronophthisis and tapeto - retinal degeneration. The author describes two patients who presented with varying degrees of retinal dystrophy and renal insufficiency in their second decade of life. Both the patients presented with severe renal failure requiring hemodialysis. The first patient had early onset progressive retinal degeneration leading to childhood blindness whereas the second patient had asymptomatic retinitis pigmentosa. These cases are presented to highlight the spectrum of eye manifestations of Senior - Loken syndrome. This report also stresses the need for fundus evaluation in patients with chronic kidney disease presenting in second decade of life even if asymptomatic.

Entities:  

Keywords:  Familial juvenile nephronophthisis; Hereditary renal - retinal dystrophy; Renal – retinal syndrome; Retinitis pigmentosa

Year:  2014        PMID: 25584255      PMCID: PMC4290257          DOI: 10.7860/JCDR/2014/9688.5120

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


  9 in total

1.  Senior-Loken syndrome with unusual manifestations.

Authors:  N P Singh; S Anuradha; S Gupta; S N Rizvi; R Arora
Journal:  J Assoc Physicians India       Date:  1998-08

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Authors:  R Janardhanan; S Krishnakumar
Journal:  J Assoc Physicians India       Date:  1997-11

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Journal:  Acta Paediatr       Date:  1961-03       Impact factor: 2.299

Review 5.  Cerebello-oculo-renal syndromes including Arima, Senior-Löken and COACH syndromes: more than just variants of Joubert syndrome.

Authors:  D Satran; M E Pierpont; W B Dobyns
Journal:  Am J Med Genet       Date:  1999-10-29

6.  Twins with senior-Loken syndrome.

Authors:  S Giridhar; R Padmaraj; Prabha Senguttuvan
Journal:  Indian J Pediatr       Date:  2006-11       Impact factor: 1.967

7.  Senior-loken syndrome with rare manifestations: a case report.

Authors:  Harikrishan K Aggarwal; Deepak Jain; Sachin Yadav; Vipin Kaverappa; Abhishek Gupta
Journal:  Eurasian J Med       Date:  2013-06

8.  Retinal manifestations in familial juvenile nephronophthisis.

Authors:  V Godel; A Iaina; P Nemet; M Lazar
Journal:  Clin Genet       Date:  1979-10       Impact factor: 4.438

9.  Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromes.

Authors:  Joseph G Gleeson; Lesley C Keeler; Melissa A Parisi; Sarah E Marsh; Phillip F Chance; Ian A Glass; John M Graham; Bernard L Maria; A James Barkovich; William B Dobyns
Journal:  Am J Med Genet A       Date:  2004-03-01       Impact factor: 2.802

  9 in total
  3 in total

1.  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

2.  Defective INPP5E distribution in NPHP1-related Senior-Loken syndrome.

Authors:  Ke Ning; Emilie Song; Brent E Sendayen; Philipp P Prosseda; Kun-Che Chang; Alireza Ghaffarieh; Jorge A Alvarado; Biao Wang; Kathryn M Haider; Nicolas F Berbari; Yang Hu; Yang Sun
Journal:  Mol Genet Genomic Med       Date:  2020-12-11       Impact factor: 2.473

3.  OFD1, as a Ciliary Protein, Exhibits Neuroprotective Function in Photoreceptor Degeneration Models.

Authors:  Juan Wang; Xin Chen; Fang Wang; Jieping Zhang; Peng Li; Zongyi Li; Jingying Xu; Furong Gao; Caixia Jin; Haibin Tian; Jingfa Zhang; Weiye Li; Lixia Lu; Guo-Tong Xu
Journal:  PLoS One       Date:  2016-05-19       Impact factor: 3.240

  3 in total

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