## Abstract We report two patients with Beare‐Stevenson syndrome. This syndrome presents craniosynostosis with or without clover‐leaf skull, craniofacial anomalies, cutis gyrata, acanthosis nigricans, prominent umbilical stump, furrowed palms and soles, genital and anal anomalies. Both female newbo
Novel FGFR2 deletion in a patient with Beare–Stevenson-like syndrome
✍ Scribed by Anne Slavotinek; Howard Crawford; Mahin Golabi; Cathy Tao; Hazel Perry; Sneha Oberoi; Karin Vargervik; Michael Friez
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 139 KB
- Volume
- 149A
- Category
- Article
- ISSN
- 1552-4825
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## Abstract Beare–Stevenson syndrome is characterized by cutis gyrata, acanthosis nigricans, skin furrows, skin tags, craniosynostosis, Crouzonoid‐like features in some cases and cloverleaf skull in others, anogenital anomalies, and prominent umbilical stump. Reported causes are an __FGFR2__ Tyr375
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