Otorhinolaryngological Findings in Patients from Southwestern Colombia with Clinical, Enzymatic and Molecular Diagnosis of Mucopolysaccharidosis II, IV-A and VI

L. Giraldo, D. Arturo-Terranova, J. M. Soto
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引用次数: 4

Abstract

 ABSTRACT Mucopolysaccharidosis is characterized by excessive accumulation of glycosaminoglycan sulfate in organs and tissues. Otorhinolaryngological and upper respiratory tract pathologies are among the earliest clinical manifestations. We realized a retrospective study of clinical and otorhinolaryngologic findings of 35 patients diagnosed with MPS type II, IV-A and VI of the Colombian southwest. As a result, we found that 64% of the patients evaluated had hearing loss, 11.3% had hypertrophy of the tonsils,17.10% short neck and macroglossia. Additionally, 47.8% of the patients presented otitis media. 20% received treatment with hearing aids. no patient reported otosclerosis or tinittus. In patients with different types of MPS, there is a high frequency and progressive tendency to suffer audiological losses and recurrent infections, so it is important an opportune diagnosis, permanent monitoring and adequate therapy to avoid the repercussion of the pathology in the quality of life of
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哥伦比亚西南部粘多糖病II型、iv型、a型和VI型临床、酶学和分子诊断患者的耳鼻喉科表现
摘要粘多糖病的特征是糖胺聚糖在器官和组织中的过度积累。耳鼻咽喉和上呼吸道病变是最早的临床表现。我们对哥伦比亚西南部35例被诊断为MPS II型、iv型、a型和VI型的患者的临床和耳鼻喉科表现进行了回顾性研究。结果,我们发现64%的患者有听力损失,11.3%的患者有扁桃体肥大,17.10%的患者有短颈和大舌。此外,47.8%的患者出现中耳炎。20%的患者接受了助听器治疗。没有患者报告耳硬化或耳鸣。不同类型MPS患者发生听力学损失和反复感染的频率高,且呈进行性趋势,因此及时诊断、长期监测和适当治疗是避免病理对患者生活质量的影响的重要因素
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
7
审稿时长
12 weeks
期刊介绍: The Journal of Inborn Errors of Metabolism and Screening (JIEMS) is an online peer-reviewed open access journal devoted to publishing clinical and experimental research in inherited metabolic disorders and screening, for health professionals and scientists. Original research articles published in JIEMS range from basic findings that have implications for disease pathogenesis and therapy, passing through diagnosis and screening of metabolic diseases and genetic conditions, and therapy development and outcomes as well. Original articles, reviews on specific topics, brief communications and case reports are welcome. JIEMS aims to become a key resource for geneticists, genetic counselors, biochemists, molecular biologists, reproductive medicine researchers, obstetricians/gynecologists, neonatologists, pediatricians, pathologists and other health professionals interested in inborn errors of metabolism and screening.
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