Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2017
The multifaceted clinical presentation of VCP-proteinopathy in a Greek family.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Ошибки и ограничения
История · было → стало
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Papadimas George K, Paraskevas George P, Zambelis Thomas, Karagiaouris Chrisostomos, Bourbouli Mara, Bougea Anastasia, Walter Maggie C, Schumacher Nicolas U, Krause Sabine, Kapaki Elisabeth
Аннотация
VCP-proteinopathy is a multisystem neurodegenerative disorder caused by mutations in valosin containing protein. Here, we report the first Greek case of VCP-proteinopathy in a 62 year old patient with a slowly progressing muscular weakness since his mid-40s and a severe deterioration during the last year. He also manifested dementia with prominent neuropsychiatric symptoms, including aggression, apathy, palilalia and obsessions. Brain MRI revealed frontal atrophy, while muscle MRI showed diffuse muscle atrophy. Family history was positive and several members of the family had been diagnosed with motor neuron disease, dementia or behavioral symptoms. Sequencing of the VCP gene revealed a pathogenic heterozygous missense mutation p.R159H. Conclusively, the present report highlights the intrafamilial variability and broadens the phenotypic spectrum of VCP-proteinopathy.