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

Scoppettuolo, Pasquale;Retif, Cecile;Kampouridis, Stelianos;Meunier, Audrey;Schulz, Joachim
(2022) Neurological Sciences — Vol. 43, n° 10, p. 6117-6120 (2022)

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Authors
  • Author
  • Retif, Cecile
    Author
  • Kampouridis, Stelianos
    Author
  • Meunier, Audrey
    Author
  • Schulz, Joachim
    Author
Abstract
Dear Editor, Leber’s hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disease causing progressive bilateral and irreversible vision loss. [...]
Affiliations
  • ULB - St Pierre HospitalNeurology Department

Citations

Scoppettuolo, P., Retif, C., Kampouridis, S., Meunier, A., & Schulz, J. (2022). MS diagnosis in a male patient with m.11778G > A Leber’s hereditary optic neuropathy. Neurological Sciences, 43(10), 6117-6120. https://doi.org/10.1007/s10072-022-06193-7 (Original work published 2022)