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Patient with a PRKAG2 mutation who developed Immunoglobulin A nephropathy: a case report
Journal article   Open access   Peer reviewed

Patient with a PRKAG2 mutation who developed Immunoglobulin A nephropathy: a case report

Michael C. Giudici, Ferhaan Ahmad and Danniele G. Holanda
European heart journal : case reports, Vol.3(2), ytz038
06/01/2019
DOI: 10.1093/ehjcr/ytz038
PMCID: PMC6601182
PMID: 31449595
url
https://doi.org/10.1093/ehjcr/ytz038View
Published (Version of record) Open Access

Abstract

Background PRKAG2 syndrome (PS) is a rare, early-onset autosomal dominant inherited disease caused by mutations in PRKAG2, the gene encoding the regulatory c2 subunit of adenosine monophosphate-activated protein kinase. PRKAG2 syndrome is associated with many cardiac manifestations, including pre-excitation, arrhythmias, left ventricular hypertrophy, and chronotropic incompetence frequently leading to early pacemaker placement. A metaanalysis of genome-wide association data in subjects with chronic kidney disease (CKD) identified a susceptibility locus in an intron of PRKAG2, which has been replicated in other studies. However, CKD has not been reported in patients with PS or mutations in PRKAG2. Case summary We report a case of a woman diagnosed at age 27 with PS when she presented with atrial fibrillation and preexcitation on electrocardiogram. By age 35, she had developed mild renal insufficiency and a biopsy demonstrated IgA nephropathy (IGAN). Discussion This is the first reported case of IGAN in a patient with PS. We discuss both PS and IGAN and the potential mechanisms by which they could be related.
 Cardiac & Cardiovascular Systems Cardiovascular System & Cardiology Life Sciences & Biomedicine Science & Technology

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