Perioperative care of a patient with Beare–Stevenson syndrome
✍ Scribed by SARA UPMEYER; MARCELLA BOTHWELL; JOSEPH D. TOBIAS
- Book ID
- 109029580
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 67 KB
- Volume
- 0
- Category
- Article
- ISSN
- 1155-5645
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## 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
## 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