Literature DB >> 17031297

X-linked retinoschisis: novel mutation in the initiation codon of the XLRS1 gene in a large family.

David Y Kim1, Kimberly A Neely, Joseph W Sassani, Tamara R Vrabec, Avinash Tantri, Arcilee Frost, Larry A Donoso.   

Abstract

PURPOSE: To describe a novel point mutation in the initiation codon of the XLRS1 gene in a large family and the clinical features of males affected with X-linked juvenile retino-schisis.
METHODS: Genealogic investigation and mutation screening of the XLRS1 gene were performed for a 4-generation family consisting of 72 members. Affected males were evaluated clinically between 1986 and 2004 with up to 18 years of follow-up.
RESULTS: We identified a novel point mutation (1A>T transversion) in the initiation codon of the XLRS1 gene in affected males resulting in an amino acid substitution of methionine to leucine (Met1Leu), therefore abolishing the translation initiation Met codon.
CONCLUSION: Identification of the disease-causing mutation in this family with long-term follow-up allows for earlier and more accurate identification of individuals at risk for this inherited progressive macular degeneration, provides for more accurate genetic counseling, and contributes to our understanding of the pathophysiology of this disorder.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 17031297     DOI: 10.1097/01.iae.0000224321.93502.a3

Source DB:  PubMed          Journal:  Retina        ISSN: 0275-004X            Impact factor:   4.256


  4 in total

1.  Molecular mechanisms leading to null-protein product from retinoschisin (RS1) signal-sequence mutants in X-linked retinoschisis (XLRS) disease.

Authors:  Camasamudram Vijayasarathy; Ruifang Sui; Yong Zeng; Guoxing Yang; Fei Xu; Rafael C Caruso; Richard A Lewis; Lucia Ziccardi; Paul A Sieving
Journal:  Hum Mutat       Date:  2010-11       Impact factor: 4.878

2.  Null retinoschisin-protein expression from an RS1 c354del1-ins18 mutation causing progressive and severe XLRS in a cross-sectional family study.

Authors:  Camasamudram Vijayasarathy; Lucia Ziccardi; Yong Zeng; Nizar Smaoui; Rafael C Caruso; Paul A Sieving
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-05-27       Impact factor: 4.799

3.  Genetic screening for OPA1 and OPA3 mutations in patients with suspected inherited optic neuropathies.

Authors:  Patrick Yu-Wai-Man; Suma P Shankar; Valérie Biousse; Neil R Miller; Lora J H Bean; Bradford Coffee; Madhuri Hegde; Nancy J Newman
Journal:  Ophthalmology       Date:  2010-10-30       Impact factor: 12.079

4.  X-Linked Retinoschisis: Phenotypic Variability in a Chinese Family.

Authors:  Yangyan Xiao; Xiao Liu; Luosheng Tang; Xia Wang; Terry G Coursey; Terry Coursy; Xiaojian Guo; Zhuo Li
Journal:  Sci Rep       Date:  2016-01-29       Impact factor: 4.379

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.