Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy

BACKGROUND: Patients with a rare genetic disease may receive renal transplantation (KTx) without a correct diagnosis of causal nephropathy and therefore develop unexpected and even severe complications. Aim of the study was to describe the cases of rare genetic disorders diagnosed after KTx, in order to draw clinical lessons for the transplant physician. METHODS: We retrospectively assessed all patients who had received a diagnosis of a rare genetic disorder after KTx. RESULTS: In our Center, more than 30% (278/911) of KTx recipients were diagnosed with a causal nephropathy: prevalence of rare genetic disorders in this group was 4.32% (12/278), including 2,8 dihydroxyadeninuria (2,8 DHA)-disease (n=2), HNF-1B associated nephropathy (n=2), UMOD-related nephropathy (n=5), Fabry disease (n=1), INF2 focal segmental glomerulosclerosis (n=1) and Senior-Loken syndrome (n=1). 2,8 DHA-nephropathy relapsed in both patients causing an acute renal failure and jeopardising the graft. CONCLUSIONS: KTx recipients without a diagnosis of causal nephropathy appear to be a selected population in which rare genetic diseases might be more common than expected. As even a belated diagnosis after KTx can have a significant impact on graft and patient survival and on other family members, this possibility should be evaluated in KTx recipients without a known causal nephropathy.