肾病综合征:一名 CD151 四蛋白缺陷患者的胫前表皮松解症:病例报告。

IF 2 Q2 MEDICINE, GENERAL & INTERNAL International Journal of Health Sciences-IJHS Pub Date : 2024-01-01
Khamisa Almokali, Hissah Alshalawi, Marwh G Aldriwesh, Raniah S Alotibi
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引用次数: 0

摘要

肾病综合征(NS)-大疱性表皮松解症(EB)感音神经性耳聋综合征是一种常染色体隐性遗传的罕见疾病,由染色体 11p15.5 上的 CD151 基因同源突变引起。在本报告中,我们讨论了一例罕见的沙特籍遗传综合征患者,该患者表现为 NS 和 EB。全基因组测序结果表明,CD151 基因中发现了一个同源致病变体(c.493C>T p.(Arg165*) ,这与常染色体隐性肾病伴胫骨前 EB 和耳聋综合征的基因诊断一致。研究结果强调,即使是单一的基因型也会导致不同的表型表现,因此有必要评估该疾病对患者的多效应影响,这种影响可从严重到轻微不等。本病例报告强调了 CD151 基因突变患者可能出现的巨大表型差异,为相关文献增添了新的内容。
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Nephrotic syndrome: Pretibial epidermolysis bullosa in a patient with CD151 tetraspanin defect: A case report.

Nephrotic syndrome (NS)-epidermolysis bullosa (EB) sensorineural deafness syndrome is an autosomal recessive rare genetic disease caused by a CD151 gene homozygous mutation on chromosome 11p15.5. In this report, we discuss a rare case related to a Saudi patient with genetic syndrome who presented with NS and EB. Whole genome sequencing results indicated a homozygous pathogenic variant identified in the CD151 gene (c.493C>T p.(Arg165*), which was consistent with a genetic diagnosis of autosomal recessive nephropathy with pretibial EB and deafness syndrome. The findings emphasize that even a single genotype can result in variable phenotypic expression, necessitating the assessment of the pleiotropic effects of the disease on the patient, which can range from severe to mild. This case report adds to the literature by highlighting the considerable phenotypic variation that can be present in patients with the CD151 mutation.

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来源期刊
International Journal of Health Sciences-IJHS
International Journal of Health Sciences-IJHS MEDICINE, GENERAL & INTERNAL-
自引率
15.00%
发文量
49
审稿时长
8 weeks
期刊最新文献
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