Endosteal hyperostosis

Worth syndrome, also known as benign form of Worth hyperostosis corticalis generalisata with torus platinus, autosomal dominant osteosclerosis, autosomal dominant endosteal hyperostosis or Worth disease, is a rare autosomal dominant congenital disorder that is caused by a mutation in the LRP5 gene. It is characterized by increased bone density and benign bony structures on the palate. [Source: Wikipedia ]

Synonyms
Hyperostosis corticalis generalisata
Is A
Osteosclerosis
Subtypes
Endosteal hyperostosis van Buchem type
Endosteal hyperostosis Worth type
May Be Caused by
Nakamura disease