MS diagnosis in a male patient with m.11778G > A Leber's hereditary optic neuropathy

Neurol Sci. 2022 Oct;43(10):6117-6120. doi: 10.1007/s10072-022-06193-7. Epub 2022 Jun 11.

Authors

Pasquale Scoppettuolo¹, Cecile Retif², Stelianos Kampouridis³, Audrey Meunier⁴, Joachim Schulz²

Affiliations

¹ Neurology Department, St Pierre Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium. Pasquale.scoppettuolo@gmail.com.
² Neurology Department, St Pierre Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium.
³ Radiology Department, St Pierre Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium.
⁴ Ophtamology Department, St Pierre Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium.

PMID: 35690699
DOI: 10.1007/s10072-022-06193-7

No abstract available

Publication types

Letter

MeSH terms

DNA, Mitochondrial / genetics
Humans
Male
Mitochondria
Mutation
Optic Atrophy, Hereditary, Leber* / diagnosis
Optic Atrophy, Hereditary, Leber* / genetics

Substances

DNA, Mitochondrial