Machado Telma, Cortinhal Telmo, Carvalho Ana Luísa, Teixeira-Marques Francisco, Silva Rufino, Murta Joaquim, Marques João Pedro
Ophthalmology Department, Centro Hospitalar e Universitário de Coimbra (CHUC), Hospitais da Universidade de Coimbra (HUC), ULS Coimbra, Praceta Prof. Mota Pinto, 3000-075, Coimbra, Portugal.
Medical Genetics Department, Hospital Pediátrico de Coimbra (HPC), ULS Coimbra, Coimbra, Portugal.
Orphanet J Rare Dis. 2025 Jan 14;20(1):22. doi: 10.1186/s13023-025-03542-5.
Syndromic genetic disorders affecting vision can also cause hearing loss, and Usher syndrome is by far the most common etiology. However, many other conditions can present dual sensory impairment. Accurate diagnosis is essential for providing patients with genetic counseling, prognostic information, and appropriate resources. This study aimed to describe the genetic profile of combined inherited deaf-blindness in Portugal.
This was a cross-sectional study conducted at a tertiary hospital in Portugal. Patients were identified through the national, web-based inherited retinal dystrophies registry (IRD-PT, retina.com.pt). Demographics, clinical, and genetic data were retrieved from individual patient records. Genetic variants were classified according to the American College of Medical Genetics and Genomics; only likely pathogenic or pathogenic variants were considered relevant for solved cases.
Eighty-four patients (58.3% males; mean age 40.0 ± 17.9 years) from 71 families were included. Usher syndrome was the most frequent etiology (71.4%) followed by Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract syndrome (6.0%), Autosomal dominant optic atrophy plus (4.8%) and cone-rod dystrophy and hearing loss (4.8%). Other less frequent etiologies included Alport syndrome (2.4%), Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (2.4%), Heimler syndrome (2.4%), Senior-Loken syndrome (1.2%), Waardenburg syndrome (1.2%), Maternally inherited diabetes and deafness (1.2%), and Stickler syndrome (1.2%). The overall diagnostic yield of deleterious variants in our deaf-blind cohort was 73.2%. A total of 55 genetic variants were identified across 16 different genes; 11 of these variants are novel and herein reported for the first time.
This is the first study to describe the genetic profile of patients with dual sensory impairment in Portugal, highlighting the genetic heterogeneity associated with inherited deaf-blindness. Usher syndrome was the most prevalent cause in this cohort. Nevertheless, several other less frequent causes must also be considered. This study showed a high diagnostic yield and reported 11 novel genetic variants, thereby contributing to expand the mutational spectrum of these conditions.
影响视力的综合征性遗传疾病也可导致听力丧失,而尤塞综合征是目前最常见的病因。然而,许多其他病症也可出现双重感觉障碍。准确诊断对于为患者提供遗传咨询、预后信息和适当资源至关重要。本研究旨在描述葡萄牙遗传性聋盲合并症的基因概况。
这是一项在葡萄牙一家三级医院进行的横断面研究。通过基于网络的全国遗传性视网膜营养不良登记处(IRD-PT,retina.com.pt)识别患者。从个体患者记录中检索人口统计学、临床和基因数据。基因变异根据美国医学遗传学与基因组学学会进行分类;仅可能致病或致病的变异被认为与确诊病例相关。
纳入了来自71个家庭的84名患者(男性占58.3%;平均年龄40.0±17.9岁)。尤塞综合征是最常见的病因(71.4%),其次是多神经病、听力丧失、共济失调、色素性视网膜炎和白内障综合征(6.0%)、常染色体显性遗传性视神经萎缩加(4.8%)以及锥杆营养不良和听力丧失(4.8%)。其他较不常见的病因包括阿尔波特综合征(2.4%)、线粒体肌病、脑病、乳酸性酸中毒和卒中样发作(2.4%)、海姆勒综合征(2.4%)、西尼尔-洛肯综合征(1.2%)、瓦登伯革综合征(1.2%)、母系遗传的糖尿病和耳聋(1.2%)以及斯蒂克勒综合征(1.2%)。我们的聋盲队列中有害变异的总体诊断率为73.2%。共在16个不同基因中鉴定出55个基因变异;其中11个变异是新发现的,首次在此报告。
这是第一项描述葡萄牙双重感觉障碍患者基因概况的研究,突出了与遗传性聋盲相关的基因异质性。尤塞综合征是该队列中最常见的病因。然而,但也必须考虑其他一些较不常见的病因。本研究显示出较高的诊断率,并报告了11个新的基因变异,从而有助于扩大这些病症的突变谱。