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Skull in Apert-Crouzon syndrome, X-ray

Skull in Apert-Crouzon syndrome, X-ray

C009/5420

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Credit

ZEPHYR / SCIENCE PHOTO LIBRARY ZEPHYR / SCIENCE PHOTO LIBRARY

Caption

Coloured X-ray (side view) of the peaked skull (turicephalic) in an adult patient with Apert-Crouzon syndrome. This inherited disorder, a mutation of the gene FGFR2, is a form of craniosynostosis.

Release details

Model release not required. Property release not available.

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