Skull in Apert-Crouzon syndrome, X-ray

Skull in Apert-Crouzon syndrome, X-ray

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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.

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Keywords: abnormal, adult patient, apert, apert-crouzon syndrome, colour, coloured, condition, congenital, craniosynostosis, crouzon, diagnosis, disease, gene fgfr2, genetic, healthcare, inherited disorder, lateral, medical, medicine, mutation, peaked skull, radiography, side view, tower, turicephalic, unhealthy, x-ray, xray

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