American Academic Scientific Research Journal for Engineering, Technology, and Sciences
Abstract
Primary tumour calcinosis is a rare condition of unknown etiopathogeny. They are transmitted in an autosomal dominant or recessive mode and predominate in the black race. Calcinoses are manifested by hydroxyapathite deposits in the dermis or hypodermis. The authors report an observation of primary tumour calcinosis associated with renal abnormalities and staturoweight retardation in an 11-year-old child
