Journal Article

Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children

Traeger-Synodinos, Joanne, Mila, Maria, Kapogiannis, Charalampos, Tilemis, Faidon-Nikolaos, Stergiou, Nikolaos, Kanaka-Gantenbein, Christina, Makrythanasis, Periklis, Kampouraki, Afroditi, Mitsioni, Andromachi, Kosma, Konstantina, Karava, Vasiliki, Tzetis, Maria, Marinakis, Nikolaos M., Christodoulaki, Vasileia

2024

Overview

Alport syndrome (AS) is a hereditary glomerulopathy due to pathogenic variants in COL4A3, COL4A4, and COL4A5. Treatment with Renin–Angiotensin–Aldosterone System (RAAS) inhibitors can delay progression to end stage renal disease (ESRD). From 2018 until today, we performed Whole Exome Sequencing (WES) in 19 patients with AS phenotype with or without positive family history. Fourteen of these patients were children. Genetic testing was extended to family members at risk. All patients received a genetic diagnosis of AS: five X-linked AS (XLAS) males, five X-linked AS (XLAS) females, six autosomal dominant AS (ADAS), and one autosomal recessive AS (ARAS). After cascade screening four XLAS males and eight XLAS females, six ADAS and three ARAS heterozygotes were added to our initial results. Fifteen patients were eligible to start treatment with RAAS inhibitors after their diagnosis. All XLAS female patients, ARAS heterozygotes, and ADAS have been advised to be followed up, so that therapeutic intervention can begin in the presence of microalbuminuria. Genetic diagnosis of AS ensures early therapeutic intervention and appropriate follow up to delay progression to chronic kidney disease, especially in thet pediatric population.

• Publisher: MDPI AG,MDPI
• Subject: Adolescent / Adult / albuminuria / Aldosterone / Alport syndrome / Alport's syndrome / Analysis / Angiotensin / Biopsy / Care and treatment / Child / Child, Preschool / Children / Collagen Type IV - genetics / Development and progression / Diagnosis / Early Diagnosis / Exome Sequencing / Families & family life / family / Family medical history / Female / Females / Genetic aspects / Genetic screening / Genetic testing / Genetic Testing - methods / Genetic variation / Genetics / Genomics / Genotype & phenotype / glomerulopathy / Health aspects / Hearing loss / Hematuria / heterozygosity / Heterozygotes / Humans / Infant / Kidney diseases / Kidney Failure, Chronic - diagnosis / Kidney Failure, Chronic - genetics / Male / Microscopy / Mutation / Nephritis, Hereditary - diagnosis / Nephritis, Hereditary - genetics / Nephrology / Patients / Pediatrics / Phenotype / Phenotypes / Population genetics / Renin / risk / therapeutics / Whole genome sequencing