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Bohring-Opitz Syndrome / ASXL1BohringOpitz
2025-02-28

Bohring-Opitz Syndrome - more than you can IMAGINE

BOHRING-0PITZ SYNDROME 2025 © MORE THAN YOU CAN IMAGINE Bohring-Opitz syndrome is a genetic condition caused by the De Novo Mutation of the ASXL1 gene. It's an extremely rare syndrome; there are around 350 people affected with this disease worldwide. www.bohring-opitz.org #RareDiseaseDay Visit our interactive visual aid about Bohring-Opitz Syndrome. Not every child will have all the classic physical characteristics, and the variation in level of development from one child to the next can be great.

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