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A 5-year-old boy with a history of global developmental delay was diagnosed with influenza A per his PCP and presented to a local hospital ED with five days of lethargy, poor PO intake, decreased urine output, and fever. He was transferred to the closest specialty pediatric hospital where an MRI revealed decreased signal in the basal ganglia, and an EEG showed slowing consistent with metabolic versus infectious encephalopathy. A genetic work-up noted significant heteroplasmy for mutation of the m.3243A>G MT-ATP6 gene, which is associated with MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes) syndrome.
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Drs. Sinha, Kremm, and Robbins report no relationships with third party entities producing health care goods and services.
All presenters disclosure of relevant financial relationships with any entity producing, marketing, re-selling, or distributing health care goods or services, used on, or consumed by, patients is listed above. No other planners, members of the planning committee, speakers, presenters, authors, content reviewers and/or anyone else in a position to control the content of this education activity have relevant financial relationships to disclose.
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Release Date: 2/16/2018 | Last Modified On: 2/16/2018 | Expires: 2/16/2019