Stickler syndrome is a group of hereditary conditions characterized by a distinctive facial appearance, eye abnormalities, hearing loss, and joint problems.
Stickler syndrome (hereditary progressive arthro-ophthalmopathy) is a group of genetic disorders affecting connective tissue, specifically collagen. 
Stickler syndrome is a genetic disorder caused by mutations in genes that are responsible for forming collagen, proteins which add strength and elasticity to ...
Stickler syndrome is a genetic disorder that can cause serious vision, hearing and joint problems. Also known as hereditary progressive arthro-ophthalmopathy ...
stickler gb, belau pg, farrell fj, jones jd, pugh dg, steinberg ag, ward le. hereditary progressive arthro-ophthalmopathy. mayo clin proc. 1965 jun; 40:433–455.
Stickler syndrome refers to a group of disorders of connective tissue. Connective tissue, which is the material between cells of the body that gives the ...
Stickler’s syndrome is an autosomal dominant connective tissue disorder also known as hereditary progressive arthro-ophthalmopathy. It is estimated to affect 1 in ...
Stickler Involved People (SIP) - the support group for those with Stickler Syndrome
Symptoms of Stickler Syndrome. The facial features of babies with Stickler syndrome vary significantly. Some babies with Stickler syndrome are born with Pierre Robin ...
The signs and symptoms of Stickler syndrome — and the severity of those signs and symptoms — can vary widely from person to person. Eye problems.