نتایج جستجو برای: pantothenate kinase associated neurodegeneration

تعداد نتایج: 1714897  

2016
Raquel Quimas Molina da Costa Rogério Paysano Marrocos Marco Antonio Araujo Leite Fabio Henrique Gobbi Porto

The atypical form of Pantothenate Kinase-Associated Neurodegeneration (PKAN) tends to present at around the age of 14 years, has a heterogeneous presentation with extrapyramidal symptoms, and approximately one third of patients exhibit psychiatric problems. This paper reports the case of a patient with apparent typical symptoms of Tourette syndrome. However, the severity and poor response to tr...

2016
Daniel I Orellana Paolo Santambrogio Alicia Rubio Latefa Yekhlef Cinzia Cancellieri Sabrina Dusi Serena G Giannelli Paola Venco Pietro G Mazzara Anna Cozzi Maurizio Ferrari Barbara Garavaglia Stefano Taverna Valeria Tiranti Vania Broccoli Sonia Levi

Pantothenate kinase-associated neurodegeneration (PKAN) is an early onset and severely disabling neurodegenerative disease for which no therapy is available. PKAN is caused by mutations in PANK2, which encodes for the mitochondrial enzyme pantothenate kinase 2. Its function is to catalyze the first limiting step of Coenzyme A (CoA) biosynthesis. We generated induced pluripotent stem cells from ...

Journal: :AJNR. American journal of neuroradiology 2006
M Koyama A Yagishita

We report a case of pantothenate kinase-associated neurodegeneration with increased regional cerebral blood flow (rCBF) in bilateral lentiform nuclei on technetium Tc-99m ethyl cysteinate dimer single-photon emission CT (ECD-SPECT). A 6-year-old boy presented with opisthotonus. T2*-weighted MR images revealed areas of marked hypointensity with a hyperintense focus in bilateral globus pallidus, ...

2014
Peter Johnson Roxanne Melbourne-Chambers Nilesh Desai Emma Greenaway

We present a case of an eleven-year-old boy presenting with progressive extrapyramidal signs and dementia. His imaging findings demonstrated the classic eye-of-the-tiger sign on T2W magnetic resonance imaging. He was diagnosed with pantothenate kinase-associated neurodegeneration (PKAN). This is a rare autosomal recessive inborn error of coenzyme A metabolism, caused by mutations in PANK2. This...

2010
Maria Livia Fantini Giovanni Cossu Andrea Molari Monia Cabinio Ozlem Uyanik Roberto Cilia Maurizio Melis Angelo Antonini Luigi Ferini-Strambi

Pantothenate kinase-associated neurodegeneration (PKAN) is a familial or sporadic disease characterized by extrapyramidal and corticospinal signs with dementia. Patients show iron accumulation in the basal ganglia, with neuronal loss and gliosis. A mutation of pantothenate kinase (PANK2) gene localized on chromosome 20p13 has been described in familiar forms, as well as in sporadic patients. We...

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