Alkaptonuria With Sequential Various Orthopedic Mani Festations – A Case Report

Alkaptonuria is a rare, autosomal recessive, inborn, metabolic disorder that causes skeletal and extra-skeletal manifestations. This case report describes a 48-year-old man with alkaptonuria who presented with sequential various orthopedic manifestations within seven yeas duration. The clinical diagnosis and treatment are also discussed.