Bonnet–Dechaume–Blanc syndrome
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Bonnet–Dechaume–Blanc syndrome

Bonnet–Dechaume–Blanc syndrome (also known as "Wyburn–Mason syndrome") is a rare condition characterized by a vascular malformation extending from the craniofacial to the orbital regions and brain.

It was characterized in 1938. The term "Wyburn–Mason syndrome" derives from a characterization made in 1943.

It is sometimes considered a phakomatosis.

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