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This condition is called porphyria (poor-FEER-ee-a). In most cases, Phosphoglycerate Kinase Deficiency is inherited as an X-linked genetic trait. Other neurologic findings may include cerebellar signs, pyramidal tract signs, extrapyramidal signs, corticla visual defects, abnormal extraocular movements, lower motor neuron signs, vestibular dysfunction, seizures, sensory deficits, and autonomic abnormalities. (Johnson, 2005) Routine laboratory findings are not helpful.
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