Literature DB >> 33068213

Novel biallelic TRPM1 variants in an elderly patient with complete congenital stationary night blindness.

Takaaki Hayashi1,2, Kei Mizobuchi3, Shinsuke Kikuchi3,4, Tadashi Nakano3.   

Abstract

BACKGROUND: Little is known about whether patients with complete congenital stationary night blindness (CSNB) maintain visual function throughout their lifetime. The purpose of this report was to describe clinical and genetic features of an elderly female patient with complete CSNB that we followed for 5 years.
METHODS: Molecular genetic analysis using whole-exome sequencing (WES) was performed to detect disease-causing variants. We performed a comprehensive ophthalmic examination including full-field electroretinography (ERG).
RESULTS: In the patient, WES identified two novel variants (c.1034delT; p.Phe345SerfsTer16 and c.1880T>A; p.Met627Lys) in the TRPM1 gene. Her unaffected daughter has one of the variants. The patient reported that her visual acuity has remained unchanged since elementary school. At the age of 68 years old, fundus and fundus autofluorescence imaging showed no remarkable findings except for mild myopic changes. Goldmann perimetry showed preserved visual fields with all V-4e, I-4e, I-3e and I-2e isopters. Optical coherence tomography demonstrated preserved retinal thickness and lamination. Rod ERG showed no response; bright-flash ERG showed an electronegative configuration with minimally reduced a-waves, and cone and 30-Hz flicker ERG showed minimally reduced responses. Overall, the ERG findings of ON bipolar pathway dysfunction were consistent with complete CSNB.
CONCLUSIONS: This is the oldest reported patient with complete CSNB and biallelic TRPM1 variants. Our ophthalmic findings suggest that some patients with TRPM1-related CSNB may exhibit preserved retinal function later in life.

Entities:  

Keywords:  Autosomal recessive inheritance; Congenital stationary night blindness; Full-field electroretinography; Retina; TRPM1 gene

Mesh:

Substances:

Year:  2020        PMID: 33068213     DOI: 10.1007/s10633-020-09798-5

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN: 0012-4486            Impact factor:   2.379


  26 in total

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5.  The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

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6.  Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

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7.  Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.

Authors:  Isabelle Audo; Kinga Bujakowska; Elise Orhan; Charlotte M Poloschek; Sabine Defoort-Dhellemmes; Isabelle Drumare; Susanne Kohl; Tien D Luu; Odile Lecompte; Eberhart Zrenner; Marie-Elise Lancelot; Aline Antonio; Aurore Germain; Christelle Michiels; Claire Audier; Mélanie Letexier; Jean-Paul Saraiva; Bart P Leroy; Francis L Munier; Saddek Mohand-Saïd; Birgit Lorenz; Christoph Friedburg; Markus Preising; Ulrich Kellner; Agnes B Renner; Veselina Moskova-Doumanova; Wolfgang Berger; Bernd Wissinger; Christian P Hamel; Daniel F Schorderet; Elfride De Baere; Dror Sharon; Eyal Banin; Samuel G Jacobson; Dominique Bonneau; Xavier Zanlonghi; Guylene Le Meur; Ingele Casteels; Robert Koenekoop; Vernon W Long; Francoise Meire; Katrina Prescott; Thomy de Ravel; Ian Simmons; Hoan Nguyen; Hélène Dollfus; Olivier Poch; Thierry Léveillard; Kim Nguyen-Ba-Charvet; José-Alain Sahel; Shomi S Bhattacharya; Christina Zeitz
Journal:  Am J Hum Genet       Date:  2012-02-10       Impact factor: 11.025

8.  Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.

Authors:  Zheng Li; Panagiotis I Sergouniotis; Michel Michaelides; Donna S Mackay; Genevieve A Wright; Sophie Devery; Anthony T Moore; Graham E Holder; Anthony G Robson; Andrew R Webster
Journal:  Am J Hum Genet       Date:  2009-10-29       Impact factor: 11.025

9.  Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.

Authors:  Maria M van Genderen; Mieke M C Bijveld; Yvonne B Claassen; Ralph J Florijn; Jillian N Pearring; Francoise M Meire; Maureen A McCall; Frans C C Riemslag; Ronald G Gregg; Arthur A B Bergen; Maarten Kamermans
Journal:  Am J Hum Genet       Date:  2009-11-05       Impact factor: 11.025

10.  TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.

Authors:  Isabelle Audo; Susanne Kohl; Bart P Leroy; Francis L Munier; Xavier Guillonneau; Saddek Mohand-Saïd; Kinga Bujakowska; Emeline F Nandrot; Birgit Lorenz; Markus Preising; Ulrich Kellner; Agnes B Renner; Antje Bernd; Aline Antonio; Veselina Moskova-Doumanova; Marie-Elise Lancelot; Charlotte M Poloschek; Isabelle Drumare; Sabine Defoort-Dhellemmes; Bernd Wissinger; Thierry Léveillard; Christian P Hamel; Daniel F Schorderet; Elfride De Baere; Wolfgang Berger; Samuel G Jacobson; Eberhart Zrenner; José-Alain Sahel; Shomi S Bhattacharya; Christina Zeitz
Journal:  Am J Hum Genet       Date:  2009-11-05       Impact factor: 11.025

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5.  Clinical and Genetic Characteristics of Korean Congenital Stationary Night Blindness Patients.

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