Title of article :
TRH therapy in a patient with juvenile Alexander disease
Author/Authors :
Keiko Ishigaki، نويسنده , , Yasushi Ito، نويسنده , , Yukio Sawaishi، نويسنده , , Kayano Kodaira، نويسنده , , Makoto Funatsuka، نويسنده , , Nozomi Hattori، نويسنده , , Kazutoshi Nakano، نويسنده , , Kayoko Saito، نويسنده , , Makiko Osawa، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
5
From page :
663
To page :
667
Abstract :
Alexander disease is a rare disorder of the central nervous system caused by a de novo mutation in the glial fibrillary acidic protein (GFAP) gene. Unlike the much more common infantile form, the juvenile form is slowly progressive with bulbar, pyramidal and cerebellar signs. Herein, we report a 9-year old Japanese girl suffering from frequent vomiting, slurred speech and truncal ataxia. Juvenile Alexander disease was diagnosed by genetic analysis, which detected a novel GFAP mutation, D360V. We also describe our clinical success in treating this patient with thyrotropin releasing hormone (TRH).
Keywords :
Juvenile Alexander disease , Novel GFAP mutation , Thyrotropin releasing hormone (TRH) therapy , Cerebellar ataxia
Journal title :
Brain and Development
Serial Year :
2006
Journal title :
Brain and Development
Record number :
495046
Link To Document :
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