A Novel Mutation in a Kazakh Family with X-Linked Alport Syndrome

Barshagul T. Baikara, Elena V. Zholdybayeva, Saule Rakhimova, Nazym Bakytbekovna Nigmatullina, Kuvat T. Momynaliev, Yerlan M. Ramankulov

PLoS ONE, 2015

Full text Open access: Gold Metadata (CSL-JSON)

DOI 10.1371/journal.pone.0132010

Data confidence 85 high

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Abstract

Alport syndrome is a genetic condition that results in hematuria, progressive renal impairment, hearing loss, and occasionally lenticonus and retinopathy. Approximately 80% of Alport syndrome cases are caused by X-linked mutations in the COL4A5 gene encoding type IV collagen. The objective of this study was to define the SNP profiles for COL4A5 in patients with hereditary nephritis and hematuria. For this, we examined four subjects from one Kazakh family clinically affected with X-linked Alport syndrome due to COL4A5 gene mutations. All 51 exons of the COL4A5 gene were screened by linkage analysis and direct DNA sequencing, resulting in the identification of a novel mutation (G641E) in exon 25. The mutation was found only in two affected family individuals but was not present in healthy family members or 200 unrelated healthy controls. This result demonstrates that this novel mutation is pathogenic and has meaningful implications for the diagnosis of patients with Alport syndrome.