Autosomal dominant Alport syndrome due to a COL4A4 mutation with an additional ESPN variant detected by whole-exome analysis

被引:0
作者
Yuichiro Izumi
Ami Hamaguchi
Rei Miura
Terumasa Nakagawa
Miyuki Nakagawa
Ken Saida
Noriko Miyake
Yu Nagayoshi
Yutaka Kakizoe
Taku Miyoshi
Yukimasa Kohda
Yohei Misumi
Naomichi Matsumoto
Yukio Ando
Masashi Mukoyama
机构
[1] Kumamoto University Graduate School of Medical Sciences,Department of Nephrology
[2] Yokohama City University Graduate School of Medicine,Department of Human Genetics
[3] Kumamoto University Graduate School of Medical Sciences,Department of Neurology
来源
CEN Case Reports | 2020年 / 9卷
关键词
Alport syndrome; Type IV collagen α4 (; ); Espin (; ); Sensorineural hearing loss; Whole-exome analysis;
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摘要
Alport syndrome (AS) is a rare hereditary disease that presents with chronic kidney disease and sensorineural hearing loss, and is diagnosed by its clinical features, pathological features on renal tissue, and mode of inheritance. We report a woman in her 20 s who exhibited persistent haematuria with normal renal function and sensorineural hearing loss. Her family members exhibited the same clinical findings among three generations and were suspected of having autosomal dominant AS (ADAS). Renal biopsy showed minor glomerular abnormalities on light microscopy and extensive thinning of the glomerular basement membrane on electron microscopy. Whole-exome analysis revealed a known COL4A4 (type IV collagen α4) mutation (c. 2510 G > C: p. Gly837Ala). Two pedigrees with the same variant have been reported previously, one as ADAS and the other as autosomal recessive AS. However, these two cases exhibited no sensorineural hearing loss. The analysis in the present case revealed another missense variant in ESPN (Espin), an actin-bundling protein, which is a causative gene for sensorineural hearing loss. Although the pathophysiological significance of this novel missense variant needs to be clarified, computational analysis predicted that the variant creates a new phosphorylation site for protein kinase C. Our case suggests a possible association of hereditary sensorineural hearing loss with ADAS. Whole-exome analysis should be considered to diagnose hereditary and multiple-organ disorders.
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页码:59 / 64
页数:5
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