Stickler syndrome, type I, nonsyndromic ocular

Stickler syndrome, type I, nonsyndromic ocular is a rare genetic disorder that primarily affects the eyes. Although detailed definition information is not available, this condition is known as an atypical form of Stickler syndrome and is often described as predominantly ocular. Some descriptions also refer to rhegmatogenous retinal detachment, highlighting that eye-related complications may be an important aspect of the condition. The condition is linked to changes in the COL2A1 gene and follows an autosomal dominant pattern of inheritance. Due to the limited detailed information currently available, further research is needed to fully understand the range of signs and symptoms in people with this condition.

Information about symptoms is currently limited for this condition.

This condition has a genetic cause. It is associated with changes in the COL2A1 gene and is inherited in an autosomal dominant manner, as suggested by the available information. More detailed explanations of its causes are limited in the current sources.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research and future directions is currently limited for this condition.