Ullrich congenital muscular dystrophy 1B

Ullrich congenital muscular dystrophy 1B is a rare inherited condition that affects muscle strength and structure. It is considered one of the congenital muscular dystrophies and is linked to changes in the COL6A2 gene. Detailed information about the full range of signs and progression is limited, and ongoing research continues to enhance understanding of the condition.

Information about symptoms is currently limited for this condition.

Ullrich congenital muscular dystrophy 1B is associated with genetic changes in the COL6A2 gene. These alterations affect muscle development and function. More detailed explanations of genetic risk factors or mechanisms are currently limited.

Information about treatment options and management approaches 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.