Explore: Stickler Syndrome

connective tissue, specifically collagen. Stickler syndrome is a subtype of collagenopathy, types II and XI. Stickler syndrome is characterized by distinctive facial

large, joints and the mouth and facial structures. Marshall syndrome and Stickler syndrome closely resemble each other; in fact they are so similar, some

well as rare skeletal syndromes such as Bruck syndrome, hypophosphatasia, geroderma osteodysplasticum, and Ehlers–Danlos syndrome. Various forms of osteoporosis

in the characteristic signs and symptoms of OSMED. Stickler syndrome (COL11A2): Stickler syndrome is a disorder that causes problems with skeletal development

losses (associated with Types II and III Stickler syndrome) is present in about 80% of patients with Stickler syndrome. However, other patients are also susceptible

disorder or syndrome. Disorders associated with PRS include Stickler syndrome, DiGeorge syndrome, fetal alcohol syndrome, Treacher Collins syndrome, and Patau

SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome, and spondyloepimetaphyseal dysplasia Strudwick type. In addition

neoplasia, type 2B Shprintzen–Goldberg syndrome Stickler syndrome There is no cure for Marfan syndrome, but life expectancy has increased significantly

scientist to describe a hereditary condition now known as Stickler syndrome. Gunnar B. Stickler was born June 13, 1925, in Peterskirchen, Germany and died

Mutations in different parts of the gene may lead to deafness or Stickler syndrome type III (myopia, retinal detachment and skeletal abnormalities).[citation