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Corrigendum: Jackson–Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2


Book ID
109915711
Publisher
Nature Publishing Group
Year
1995
Tongue
English
Weight
73 KB
Volume
9
Category
Article
ISSN
1061-4036

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Fibroblast growth factor receptor (FGFR) mutations have been found in craniosynostosis syndromes with and without limb and/ or dermatologic anomalies. Ocular manifestations of FGFR2 syndromes are reported to include shallow orbits, proptosis, strabismus, and hypertelorism, but no ocular anterior cha