Worth syndrome
（重定向自Hyperostosis Corticalis Generalisata）
![Worth syndrome has an autosomal dominant pattern of inheritance.](/Images/godic/202501/19/Autosomal_dominant_-_en.svg5405.png")
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.