Sporadic idiopathic acro-osteolysis with cranio-skeletal dysplasia, polycystic kidneys and glomerulonephritis A case of the hajdu-cheney syndrome

Abstract
A case of the Hajdu-Cheney syndrome in 1515 year old boy is described. The manifestations were: 1. idiopathic progressive acro-osteolysis; 2. multiple cranio-skeletal abnormalities; and 3. polycystic kidneys complicated by a rapidly progressive glomerulonephritis.