PFAPA SYNDROME - RARE DESEASES

PFAPA syndrome



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Fibrodysplasia ossificans progressiva (FOP): what it is, symptoms and treatment
PFAPA syndrome is a rare genetic disease that develops in infancy up to five years of age. In this syndrome the child develops monthly symptoms such as fever, aphthous stomatitis or pharyngitis and adenitis. This disease is benign and the children who suffer from it go through periods of fevers that last from three to five days with intervals of 28 days