Pearls & Oy-sters: Leber Hereditary Optic Neuropathy-Plus Masquerading as Neuromyelitis Optica Spectrum Disorder in a 2-Year-Old Child.

Sunshine, Alex; Mandle, Quinton J; Cabal Herrera, Ana M; Zapanta, Bianca; Varma, Hersh; Magaña, Setty

Sunshine, Alex; Mandle, Quinton J; Cabal Herrera, Ana M; Zapanta, Bianca; Varma, Hersh; Magaña, Setty.

Afiliación

Sunshine A; From the Neurology (A.S., Q.J.M., S.M.); Pediatrics (A.M.C.H.); Genetics (B.Z.); and Ophthalmology (H.V.), Nationwide Children's Hospital.
Mandle QJ; From the Neurology (A.S., Q.J.M., S.M.); Pediatrics (A.M.C.H.); Genetics (B.Z.); and Ophthalmology (H.V.), Nationwide Children's Hospital.
Cabal Herrera AM; From the Neurology (A.S., Q.J.M., S.M.); Pediatrics (A.M.C.H.); Genetics (B.Z.); and Ophthalmology (H.V.), Nationwide Children's Hospital.
Zapanta B; From the Neurology (A.S., Q.J.M., S.M.); Pediatrics (A.M.C.H.); Genetics (B.Z.); and Ophthalmology (H.V.), Nationwide Children's Hospital.
Varma H; From the Neurology (A.S., Q.J.M., S.M.); Pediatrics (A.M.C.H.); Genetics (B.Z.); and Ophthalmology (H.V.), Nationwide Children's Hospital.
Magaña S; From the Neurology (A.S., Q.J.M., S.M.); Pediatrics (A.M.C.H.); Genetics (B.Z.); and Ophthalmology (H.V.), Nationwide Children's Hospital.

Neurology ; 101(24): e2585-e2588, 2023 Dec 12.

Article en En | MEDLINE | ID: mdl-37827846

Asunto(s)

Neuromielitis Óptica; Atrofia Óptica Hereditaria de Leber; Humanos; Preescolar; Atrofia Óptica Hereditaria de Leber/diagnóstico; Atrofia Óptica Hereditaria de Leber/genética; Neuromielitis Óptica/diagnóstico

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neuromielitis Óptica / Atrofia Óptica Hereditaria de Leber Límite: Child, preschool / Humans Idioma: En Revista: Neurology Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos

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