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Pantothenate kinase 2 deficiency: A neurodegeneration with brain iron accumulation

Pantothenate kinase 2 deficiency (previously known as Hallervorden-Spatz disease) is an unusual metabolic disorder characterized by progressive extrapyramidal dysfunction and dementia. A 27-year-old Caucasian presented with a major depression disorder and social phobia since adolescence. Patient had...

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Detalles Bibliográficos
Autores principales: Yousaf, Muhammad, Ramakrishnaiah, Raghu H., Kaushik, Chhavi, Kumar, Manoj, Shah, Chetan Chandulal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898076/
https://www.ncbi.nlm.nih.gov/pubmed/27307830
http://dx.doi.org/10.2484/rcr.v4i3.319
Descripción
Sumario:Pantothenate kinase 2 deficiency (previously known as Hallervorden-Spatz disease) is an unusual metabolic disorder characterized by progressive extrapyramidal dysfunction and dementia. A 27-year-old Caucasian presented with a major depression disorder and social phobia since adolescence. Patient had marked paranoia, auditory hallucinations, extrapyramidal dysfunction, poor memory, and gait abnormality. Laboratory tests including serum copper and ceruloplasmin were all normal. Magnetic resonance imaging (MRI) examination of the brain played an important role in the diagnosis in this patient.