Hearing impairment and renal failure associated with RMND1 mutations

Research output: Contribution to journalJournal articleResearchpeer-review

Kirstine Ravn, Mette Neland, Flemming Wibrand, Morten Duno, Elsebet Ostergaard

Recently, two research groups reported that mutations in RMND1 were associated with encephalopathy, elevated lactate, hypotonia, and in some patients seizures or myoclonia in individuals from two consanguineous families. A combined respiratory chain deficiency and a defect in mitochondrial protein translation was found. In this study, we report two siblings who are compound heterozygous for the mutations, c.713A>G and c.1003delG, in RMND1. Respiratory chain enzymatic analysis and BN-PAGE showed a combined OXPHOS deficiency. Western blot analysis indicated normal levels of RMND1, but the assembly of the RMND1 homopolymeric complex was highly impaired. The two siblings had a markedly milder phenotype and longer survival compared to previously reported patients. In addition, they had renal failure and hearing impairment. These two newly described patients contribute to delineation of the clinical spectrum associated with RMND1 aberrations.

Original languageEnglish
JournalAmerican Journal of Medical Genetics. Part A
Volume170
Issue number1
Pages (from-to)142-147
Number of pages6
ISSN1552-4825
DOIs
Publication statusPublished - Jan 2016

    Research areas

  • Adolescent, Amino Acid Sequence, Cell Cycle Proteins, Child, Child, Preschool, Female, Hearing Loss, Humans, Infant, Infant, Newborn, Male, Mitochondria, Mitochondrial Diseases, Molecular Sequence Data, Mutation, Pedigree, Protein Biosynthesis, Renal Insufficiency, Sequence Homology, Amino Acid, Case Reports

ID: 173809690