| Literature DB >> 26446305 |
Atsuhiko Handa1, Yuka Okajima2, Noriko Izumi3, Michiko Yamanaka3, Yasuyuki Kurihara2.
Abstract
Bent bone dysplasia-fibroblast growth factor receptor 2 type (BBD-FGFR2) is a recently identified skeletal dysplasia caused by specific FGFR2 mutations, characterized by craniosynostosis and prenatal bowing of the long bones. Only a few cases have been published. We report an affected fetus terminated at 21 weeks of gestation. The clinical and radiologic manifestations mostly recapitulate previous descriptions; however we suggest additional hallmarks of this disorder in early gestation. These hallmarks include distinctive short, thick clavicles and wavy ribs, as well as vertebral bodies that showed striking anteroposterior shortening. Femoral fractures were also present in our case. Although craniosynostosis is a hallmark of the disease, clinicians should be aware that craniosynostosis might not be readily apparent on plain films early in gestation.Entities:
Keywords: Bent bone dysplasia; Bowed long bones; Craniosynostosis; FGFR2; Fetus; Fibroblast growth factor receptor 2 type (BBD-FGFR2); Radiography; Skeletal dysplasia
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Year: 2015 PMID: 26446305 DOI: 10.1007/s00247-015-3465-y
Source DB: PubMed Journal: Pediatr Radiol ISSN: 0301-0449