Literature DB >> 30578507

Ciliopathy: Senior-Løken Syndrome.

Stephen H Tsang1,2, Alicia R P Aycinena3, Tarun Sharma4.   

Abstract

Senior-Løken syndrome is a rare autosomal recessive disease with a prevalence of 1:1,000,000. Retinopathy may progress as Leber congenital amaurosis (LCA), retinitis pigmentosa (RP), or sector RP (Figs. 34.1 and 34.2). Onset of photophobia, nystagmus, and hyperopia can occur in the first few years of life or later in childhood. Patients experience nephronophthisis, characterized by cystic kidney disease (medullary cystic kidney disease), reduced concentrating ability, and chronic tubulointerstitial nephritis, which progresses to end-stage renal disease. Hypertension is common.

Entities:  

Keywords:  Ciliopathy; Senior Loken syndrome; Senior-Løken syndrome

Mesh:

Year:  2018        PMID: 30578507     DOI: 10.1007/978-3-319-95046-4_34

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  6 in total

1.  Autosomal Recessive Retinitis Pigmentosa Associated with Three Novel REEP6 Variants in Chinese Population.

Authors:  Lujia Zhang; Ya Li; Litao Qin; Yu Wu; Bo Lei
Journal:  Genes (Basel)       Date:  2021-04-07       Impact factor: 4.096

Review 2.  Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies.

Authors:  Aymane Bouzidi; Hicham Charoute; Majida Charif; Ghita Amalou; Mostafa Kandil; Abdelhamid Barakat; Guy Lenaers
Journal:  Orphanet J Rare Dis       Date:  2022-05-12       Impact factor: 4.303

3.  Atypical histological abnormalities in an adult patient with nephronophthisis harboring NPHP1 deletion: a case report.

Authors:  Maiko Akira; Hitoshi Suzuki; Arisa Ikeda; Masako Iwasaki; Daisuke Honda; Hisatsugu Takahara; Hisaki Rinno; Shigeki Tomita; Yusuke Suzuki
Journal:  BMC Nephrol       Date:  2021-07-10       Impact factor: 2.388

4.  A case report of NPHP1 deletion in Chinese twins with nephronophthisis.

Authors:  Feng Chen; Limeng Dai; Jun Zhang; Furong Li; Jinbo Cheng; Jinghong Zhao; Bo Zhang
Journal:  BMC Med Genet       Date:  2020-04-19       Impact factor: 2.103

Review 5.  Leber congenital amaurosis/early-onset severe retinal dystrophy: current management and clinical trials.

Authors:  Malena Daich Varela; Thales Antonio Cabral de Guimaraes; Michalis Georgiou; Michel Michaelides
Journal:  Br J Ophthalmol       Date:  2021-03-12       Impact factor: 4.638

Review 6.  Primary Cilia and Their Role in Acquired Heart Disease.

Authors:  Zachariah E Hale; Junichi Sadoshima
Journal:  Cells       Date:  2022-03-11       Impact factor: 6.600

  6 in total

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