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Neurologic considerations in propionic acidemia
Authors:Schreiber John  Chapman Kimberly A  Summar Marshall L  Ah Mew Nicholas  Sutton V Reid  MacLeod Erin  Stagni Kathy  Ueda Keiko  Franks Jill  Island Eddie  Matern Dietrich  Peña Loren  Smith Brittany  Urv Tiina  Venditti Charles  Chakarapani Anupam  Gropman Andrea L
Institution:Department of Neurology, Children's National Medical Center, Washington, DC 20010, USA.
Abstract:Propionic acidemia (PA) is an organic acidemia which has a broad range of neurological complications, including developmental delay, intellectual disability, structural abnormalities, metabolic stroke-like episodes, seizures, optic neuropathy, and cranial nerve abnormalities. As the PA consensus conference hosted by Children's National Medical Center progressed from January 28 to 30, 2011, it became evident that neurological complications were common and a major component of morbidity, but the role of imaging and the basis for brain pathophysiology were unclear. This paper reviews the hypothesized pathophysiology, presentation and uses the best available evidence to suggest programs for treatment, imaging, and monitoring the neurological complications of PA.
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