Pearls & Oy-sters: Leber Hereditary Optic Neuropathy-Plus Masquerading as Neuromyelitis Optica Spectrum Disorder in a 2-Year-Old Child.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 37827846.
- Also identified by DOI 10.1212/WNL.0000000000207979 and PMC identifier 10791055.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
"Leber hereditary optic neuropathy (LHON-Plus)" is a phenotype of LHON that is characterized by extraocular neurologic manifestations, which may be the first manifestations of the disease.
Medical subject headings
- Optic Atrophy, Hereditary, Leber
- Neuromyelitis Optica