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Definite familial multiple system atrophy with unknown genetics.
Itoh, Kyoko; Kasai, Takashi; Tsuji, Yukiko; Saito, Kozo; Mizuta, Ikuko; Harada, Yoshinori; Sudoh, Shinji; Mizuno, Toshiki; Nakagawa, Masanori; Fushiki, Shinji.
Afiliación
  • Itoh K; Department of Pathology & Applied Neurobiology, Graduate School of Medical Sciences, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Neuropathology ; 34(3): 309-13, 2014 Jun.
Article en En | MEDLINE | ID: mdl-24397755
Multiple system atrophy (MSA) is an oligodendrogliopathy of presumably sporadic origin, characterized by prominent α-synuclein inclusions with neuronal multisystem degeneration, although a few Mendelian pedigrees have been reported. Here we report two familial cases of MSA of unknown genetic background. One patient was diagnosed as a possible MSA-C (cerebellar dysfuntion) case, and the other as clinically possible MSA-P (parkinsonism), which turned out to be definite MSA, based on a detailed autopsy. The neuropathology showed extensive deposition of α-synuclein in the glia as well as in the neurons located in the cerebral cortices and hippocampal systems, although neither multiplication of the SNCA gene or mutations in COQ2 gene were identified in the family concerned.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Atrofia de Múltiples Sistemas Tipo de estudio: Prognostic_studies Límite: Aged / Humans / Male Idioma: En Revista: Neuropathology Asunto de la revista: NEUROLOGIA / PATOLOGIA Año: 2014 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Atrofia de Múltiples Sistemas Tipo de estudio: Prognostic_studies Límite: Aged / Humans / Male Idioma: En Revista: Neuropathology Asunto de la revista: NEUROLOGIA / PATOLOGIA Año: 2014 Tipo del documento: Article País de afiliación: Japón