Uncommon case of mitochondrial disease: Mild amyotrophy of the legs and symmetrical lipomatosis of the arms
J Inherit Metab Dis
.
2025 Jan;48(1):e12820.
doi: 10.1002/jimd.12820.
Epub 2024 Nov 26.
Authors
Leslie Bercu
1
,
Patrizia Amati-Bonneau
2
,
Valérie Desquiret-Dumas
2
,
Vincent Procaccio
3
,
François Maillot
1
4
Affiliations
1
Department of Internal Medicine, University Hospital of Tours, Univ Tours, Tours, France.
2
Department of Biochemistry and Molecular Biology, CHU Angers, Angers, France.
3
Department of Genetics, CHU Angers, Univ Angers, UMR CNRS 6015-INSERM U1083, Angers, France.
4
UMR INSERM 1253 "IBraiN", University of Tours, Tours, France.
PMID:
39600123
PMCID:
PMC11670272
DOI:
10.1002/jimd.12820
No abstract available
Keywords:
lipomatosis; mitochondial diseases; mitochondrial DNA mutations.