What is Bohring-Opitz syndrome?

Bohring-Opitz Syndrome is a rare congenital disorder that is characterized by abnormal facial features, short stature, learning disability, and feeding difficulty. The pathway for causation is unknown, but some cases have been related to a genetic mutation.

How do members experience Bohring-Opitz syndrome?

*Reports may be affected by other conditions and/or medication side effects. We ask about general symptoms (anxious mood, depressed mood, fatigue, pain, and stress) regardless of condition.