• A new recessively inherited disorder composed of foveal hypoplasia, optic nerve decussation defects and anterior segment dysgenesis maps to chromosome 16q23.3-24.1
• A rare case of bilateral optic nerve sheath meningioma
• Non-arteritic anterior ischemic optic neuropathy secondary to acute primary-angle closure
• Cholesterol granuloma of the orbit: an atypical presentation
• Oculogyric crisis in a patient taking metoclopramide
• Persistent negative visual aura in migraine without headache: a case report.
• A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber?s hereditary optic neuropathy
• Myeloid sarcoma
• Spontaneous Cerebrospinal Fluid Otorrhea and Rhinorrhea in Idiopathic Intracranial Hypertension Patients
• Bilateral Internuclear Ophthalmoplegia in Multiple Sclerosis

A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber?s hereditary optic neuropathy.
Shiraishi W, Hayashi S, Kamada T, Isobe N, Yamasaki R, Murai H, Ohyagi Y, Kira JI. Mult Scler. 2013 Nov 21. [Epub ahead of print]

Los autores reportan una paciente femenina de 36 años de edad, de origen japonés con neuromielitis óptica y una mutación mitocondrial patógena para neuropatía óptica hereditaria de Leber (mutación puntual G11778A), que presentó muy mala evolución a pesar de la terapia inmunosupresora intensiva.