A Case of a 23-Year-Old Male With Leber Hereditary Optic Neuropathy With a Rare Mutation.

Lnu, Priyal; Sehgal, Vineet; Bhalla Sehgal, Lucky; Gulati, Nihal; Kapila, Saniya

Lnu, Priyal; Sehgal, Vineet; Bhalla Sehgal, Lucky; Gulati, Nihal; Kapila, Saniya.

Affiliation

Lnu P; Neurology, Sehgal's Neuro & Child Care Centre, Amritsar, IND.
Sehgal V; Neurology, Lady Hardinge Medical College, New Delhi, IND.
Bhalla Sehgal L; Neurology, Amandeep Medicity, Amritsar, IND.
Gulati N; Paediatrics, Sehgal's Neuro & Child Care Centre, Amritsar, IND.
Kapila S; General Practice, Navpreet Hospital, Amritsar, IND.

Cureus ; 14(10): e30198, 2022 Oct.

Article de En | MEDLINE | ID: mdl-36381806

Mots clés

blindness without neurological deficit; genetic eye diseases; leber hereditary optic neuropathy; mtdna disorder; mtdna mutation; rare genetic diseases; sudden loss of vision

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Prognostic_studies Langue: En Journal: Cureus Année: 2022 Type de document: Article Pays de publication: États-Unis d'Amérique

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