Fraser syndrome is a rare genetic disorder that affects multiple parts of the body. It is estimated to occur in about 1 in 100,000 to 300,000 births. Fraser syndrome often causes defects in the eyes, skin, larynx, lungs, kidneys, and skeleton. Some common features include cryptophthalmos (the eyes are covered by skin or fused shut), syndactyly (webbing or fusion of the fingers and toe... https://www.ukwebwire.com/frasier-syndrome-market-emerging-therapeutic-approaches/