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familial neuromyelitis optica: a case report and literature review
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نویسنده
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ghadiri fereshteh ,asadollahzade elnaz ,ebadi zahra ,naser moghadasi abdorreza
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منبع
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case reports in clinical practice - 2022 - دوره : 7 - شماره : 6 - صفحه:301 -305
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چکیده
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Neuromyelitis optica spectrum disorder (nmosd) is an autoimmune rare disorder that involves the endfeet of astrocytes. the role of genetics in the disease is not well known. rare cases of familial nmosd were reported worldwide. in this report, first, we presented a young man with myelitis and his cousin who suffered from this disease. then we reviewed some reports around the world about familial nmo. the prevalence of familial nmo is nearly 3%. first cases are reported from east asia. its characteristics are similar to the sporadic type. recent data suggest genetics play role in nmo.
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کلیدواژه
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neuromyelitis optica (nmo) ;familial ; myelitis
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آدرس
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tehran university of medical sciences, multiple sclerosis research center, neuroscience institute, iran, tehran university of medical sciences, multiple sclerosis research center, neuroscience institute, iran, tehran university of medical sciences, multiple sclerosis research center, neuroscience institute, iran, tehran university of medical sciences, multiple sclerosis research center, neuroscience institute, iran
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پست الکترونیکی
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abdorrezamoghadasi@gmail.com
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Authors
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