The authors report neurologic features in a large family harboring the mitochondrial DNA (mtDNA) mutation T14484C associated with Leber hereditary optic neuropathy (LHON). In the maternal line the mtDNA mutation was associated with optic neuropathy or migraine with aura or without aura and transient neurologic/visual disturbances. The segregation of familiar cases of migraine and LHON mutation broadens the clinical phenotype associated with a primary LHON mutation.

Cupini, L., Massa, R., Floris, R., Manenti, G., Martini, B., Tessa, A., et al. (2003). Migraine-like disorder segregating with mtDNA 14484 Leber hereditary optic neuropathy mutation. NEUROLOGY, 60(4), 717-719.

Migraine-like disorder segregating with mtDNA 14484 Leber hereditary optic neuropathy mutation

MASSA, ROBERTO;FLORIS, ROBERTO;MANENTI, GUGLIELMO;BERNARDI, GIORGIO;
2003-01-01

Abstract

The authors report neurologic features in a large family harboring the mitochondrial DNA (mtDNA) mutation T14484C associated with Leber hereditary optic neuropathy (LHON). In the maternal line the mtDNA mutation was associated with optic neuropathy or migraine with aura or without aura and transient neurologic/visual disturbances. The segregation of familiar cases of migraine and LHON mutation broadens the clinical phenotype associated with a primary LHON mutation.
2003
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/36 - DIAGNOSTICA PER IMMAGINI E RADIOTERAPIA
Settore MED/26 - NEUROLOGIA
English
Con Impact Factor ISI
Cupini, L., Massa, R., Floris, R., Manenti, G., Martini, B., Tessa, A., et al. (2003). Migraine-like disorder segregating with mtDNA 14484 Leber hereditary optic neuropathy mutation. NEUROLOGY, 60(4), 717-719.
Cupini, L; Massa, R; Floris, R; Manenti, G; Martini, B; Tessa, A; Nappi, G; Bernardi, G; Santorelli, F
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/67364
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