Journal Article


The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease

Abstract

Background Mutations in the RMND1 (Required for Meiotic Nuclear Division protein 1) gene have recently been linked to infantile onset mitochondrial disease characterised by multiple mitochondrial respiratory chain defects. Methods We summarised the clinical, biochemical and molecular genetic investigation of an international cohort of affected individuals with RMND1 mutations. In addition, we reviewed all the previously published cases to determine the genotype–phenotype correlates and performed survival analysis to identify prognostic factors. Results We identified 14 new cases from 11 pedigrees that harbour recessive RMND1 mutations, including 6 novel variants: c.533C>A, p.(Thr178Lys); c.565C>T, p.(Gln189*); c.631G>A, p.(Val211Met); c.1303C>T, p.(Leu435Phe); c.830+1G>A and c.1317+1G>T. Together with all previously published cases (n=32), we show that congenital sensorineural deafness, hypotonia, developmental delay and lactic acidaemia are common clinical manifestations with disease onset under 2 years. Renal involvement is more prevalent than seizures (66% vs 44%). In addition, median survival time was longer in patients with renal involvement compared with those without renal disease (6 years vs 8 months, p=0.009). The neurological phenotype also appears milder in patients with renal involvement. Conclusions The clinical phenotypes and prognosis associated with RMND1 mutations are more heterogeneous than that were initially described. Regular monitoring of kidney function is imperative in the clinical practice in light of nephropathy being present in over 60% of cases. Furthermore, renal replacement therapy should be considered particularly in those patients with mild neurological manifestation as shown in our study that four recipients of kidney transplant demonstrate good clinical outcome to date.

Attached files

Authors

Ng, Y
Aston, C
Diodato, D
Morris, A
Ulrick, N
Kmoch, S
Houšt?k, J
Martinelli, D
Haghighi, A
Atiq, M
Anton Gamero, M
Garcia-Martinez, E
Kratochvilova, H
Santra, S
Brown, R
Brown, G
Ragge, N
Monaravi, A
Pysden, K
Ravn, K
Cassey, J
Khan, A
Chakrapani, A
Vassallo, G
Simons, C
McKeever, K
O'Sullivan, S
Childs, A
Østergaard, E
Vanderver, A
Goldstein, A
Vogt, J
Taylor, R
McFarland, R

Oxford Brookes departments

Faculty of Health and Life Sciences\Department of Biological and Medical Sciences

Dates

Year of publication: 2016
Date of RADAR deposit: 2016-10-05


Creative Commons License This work is licensed under a Creative Commons Attribution 4.0 International License


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This RADAR resource is the Version of Record of The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease
This RADAR resource is the Version of Record of The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease

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