Hepatocerebral form of mitochondrial DNA depletion syndrome: novel MPV17 mutations.

Research paper by Antonella A Spinazzola, René R Santer, Orhan H OH Akman, Kostas K Tsiakas, Hansjoerg H Schaefer, Xiaoqi X Ding, Charalampos L CL Karadimas, Sara S Shanske, Jaya J Ganesh, Salvatore S Di Mauro, Massimo M Zeviani

Indexed on: 13 Aug '08Published on: 13 Aug '08Published in: Archives of neurology


Autosomal recessive mutations in MPV17 (OMIM *137960) have been identified in the hepatocerebral form of mitochondrial DNA depletion syndrome (MDS).To describe the clinical, morphologic, and genetic findings in 3 children with MPV17-related MDS from 2 unrelated families.Case report.Academic research.We identified 3 novel pathogenic mutations in 3 children.Two children were homozygous for nonsense mutation p.W120X. A third child was compound heterozygous for missense mutation p.G24W and for a macrodeletion spanning MPV17 exon 8. All patients demonstrated lactic acidosis, hypoglycemia, hepatomegaly, and progressive liver failure. Neurologic symptoms manifested at a later stage of the disease. Death occurred within the first year of life in all 3 patients.These data confirm that MPV17 mutations are associated with a 2-stage syndrome. The first symptoms are metabolic and rapidly progress to hepatic failure. This stage is followed by neurologic involvement affecting the central and peripheral systems.

More like this: