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Novel TRPM1 mutations in two Chinese families with early-onset high myopia, with or without complete congenital stationary night blindness 被引量:3
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作者 Lin Zhou Tuo Li +3 位作者 Yi-Qiao Xing Yin Li Qing-Song Wu Mao-Ju Zhang 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2016年第10期1396-1402,共7页
AIM:To investigate the relationship between high myopia [with or without complete congenital stationary night blindness(CSNB1)] and TRPM1 and NYX.METHODS: Two unrelated families with early-onset high myopia(eo HM... AIM:To investigate the relationship between high myopia [with or without complete congenital stationary night blindness(CSNB1)] and TRPM1 and NYX.METHODS: Two unrelated families with early-onset high myopia(eo HM) and 96 normal controls were recruited.Sanger sequencing or clone sequencing were used for mutation screening.Further analyses of the available family members and the 96 normal controls were subsequently conducted to obtain additional evidence of the pathogenicity of these variants.The initial diagnosis of the probands was eo HM.We performed a further comprehensive examination of the available family members after mutations were detected in TRPM1 or NYX. RESULTS: Two novel compound heterozygous mutations in TRPM1 were detected in the recruited families.The proband in family A with eo HM carried a c.2594 C 〉T missense mutation in exon 19 and a c.669 +3_669 +6del AAGT splicing mutation,which was co-segregated with CSNB1 in this family.A patient in family B with a compound heterozygous missense mutation(c.3262 G〉A and c.3250 T〉C) was detected.No mutations were found in NYX.These two identified compound heterozygous mutations were not found in the 96 normal controls.After further examination of the family members,the patients in family A could be diagnosed as eo HM with CSNB1.However due to the limited clinic data,the patient in family B cloud not clearly diagnosed as CSNB1.CONCLUSION: This study has expanded the mutation spectrum of TRPM1 for CSNB1 and additional studiesare needed to elucidate the association between isolated high myopia and TRPM1 and NYX. 展开更多
关键词 TRPM1 NYX MUTATIONS high myopia complete congenital stationary night blindness
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Night blindness due to vitamin A deficiency associated with resected adenocarcinoma of the pancreas
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作者 Andreas Kontos Hamzeh Kayhanian +1 位作者 Fatima El-Khouly Roopinder Gillmore 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2015年第1期206-207,共2页
【正】Dear Sir,W e write to present a rare case of night blindness caused by vitamin A deficiency secondary to resected adenocarcinoma of the pancreas.To our knowledge this is the first reported case of this associati... 【正】Dear Sir,W e write to present a rare case of night blindness caused by vitamin A deficiency secondary to resected adenocarcinoma of the pancreas.To our knowledge this is the first reported case of this association.A 62 year-old man presented to the eye clinic with a 12mo history of worsening nyctalopia and colour perception. 展开更多
关键词 ERG night blindness due to vitamin A deficiency associated with resected adenocarcinoma of the pancreas
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A Light-Deprivation Mouse Model Potentially for Studying the Complete Congenital Stationary Night Blindness
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作者 Chanyi Lu Qiqin Li +2 位作者 Yaoyao Li Yun Wang Yun-Feng Zhang 《World Journal of Neuroscience》 2016年第3期181-183,共3页
Current rodent models of the complete congenital stationary night blindness (CSNB1) were time- consuming in breeding and validation, which makes it imperative to find a more “easily handle” animal model to broaden o... Current rodent models of the complete congenital stationary night blindness (CSNB1) were time- consuming in breeding and validation, which makes it imperative to find a more “easily handle” animal model to broaden our understanding of this disorder. In the present study, a light-deprivation (LD) mouse model was made to validate whether it was a more “suitable” animal mode for investigating the pathogenesis of the CSNB1. Compared with controls, the LD mice exhibited a remarkable reduction in the amplitude of the dark-adapted electroretinogram (ERG) b-wave, the Max-ERG b-wave and also the oscillatory potentials (Ops), indicating an abnormal activity of rod bipolar cells in the retina. However, the ERG a-wave was relatively normal in the LD mice, which was quite consistent with what was confirmed in previously reported animal models of the CSNB1 and CSNB patients. Taken together, the LD mouse model showed CSNB1-like negative ERG responses as evidenced by the abnormal b-wave. Our study will provide a potentially useful animal model to decipher the pathogenesis of the CSNB1. 展开更多
关键词 Complete Congenital Stationary night blindness Light-Deprivation ELECTRORETINOGRAM Oscillatory Potentials
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Targeting molecular pathways for the treatment of inherited retinal degeneration 被引量:2
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作者 Meltem Kutluer Li Huang Valeria Marigo 《Neural Regeneration Research》 SCIE CAS CSCD 2020年第10期1784-1791,共8页
Inherited retinal degeneration is a major cause of incurable blindness characterized by loss of retinal photoreceptor cells.Inherited retinal degeneration is characterized by high genetic and phenotypic heterogeneity ... Inherited retinal degeneration is a major cause of incurable blindness characterized by loss of retinal photoreceptor cells.Inherited retinal degeneration is characterized by high genetic and phenotypic heterogeneity with several genes mutated in patients affected by these genetic diseases.The high genetic heterogeneity of these diseases hampers the development of effective therapeutic interventions for the cure of a large cohort of patients.Common cell demise mechanisms can be envisioned as targets to treat patients regardless the specific mutation.One of these targets is the increase of intracellular calcium ions,that has been detected in several murine models of inherited retinal degeneration.Recently,neurotrophic factors that favor the efflux of calcium ions to concentrations below toxic levels have been identified as promising molecules that should be evaluated as new treatments for retinal degeneration.Here,we discuss therapeutic options for inherited retinal degeneration and we will focus on neuroprotective approaches,such as the neuroprotective activity of the Pigment epithelium-derived factor.The characterization of specific targets for neuroprotection opens new perspectives together with many questions that require deep analyses to take advantage of this knowledge and develop new therapeutic approaches.We believe that minimizing cell demise by neuroprotection may represent a promising treatment strategy for retinal degeneration. 展开更多
关键词 ACHROMATOPSIA calcium CALPAINS CALPASTATIN congenital stationary night blindness Leber’s congenital amaurosis retinitis pigmentosa stargardt disease
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