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Rare diseases / Fibroblast growth factor receptor 2 / Antley-Bixler syndrome / Craniosynostosis / Medical genetics / Apert syndrome / Health / Medicine / Syndromes


Disease Contact details Regional Genetics Service Level 5/6, Barclay House 37 Queen Square London, WC1N 3BH
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Document Date: 2015-03-20 10:07:31

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City

London / /

/

Facility

Queen Square / /

IndustryTerm

appropriate telephone number / /

MedicalCondition

bicoronal craniosynostosis / Paternal FGFR2-related craniosynostosis syndrome / FGFR2-related isolated coronal synostosis / exceptionally rare craniosynostosis syndrome / Antley-Bixler syndrome / FGFR2-related craniosynostosis syndrome / skull deformity / same clinical syndrome / radiohumeral synostosis / FGFR2-related craniosynostosis / craniosynostosis / /

Organization

Fetal Medicine Unit / /

Person

Fiona McKay / Lyn Chitty / /

/

Position

Professor / /

SocialTag