Juvenile Paget disease

Juvenile Paget disease is a very rare form of Paget disease of the bone characterized by a general increase in bone turnover with increased bone resorption and deposition, resulting in cortical and trabecular thickening, and clinically presenting as progressive skeletal deformities, growth impairment, fractures, vertebral collapse, skull enlargement and sensorineural hearing loss.

Also known as: Hereditary Hyperphosphatasia, JPG, familial hyperphosphatasia, familial osteoectasia, hereditary hyperphosphatasia, hyperostosis corticalis deformans juvenilis, juvenile Paget disease, juvenile Paget's disease

35 clinical trials for this condition and its sub-types.