4.2 Article

Clinical and radiographic delineation of Bent Bone Dysplasia-FGFR2 type or Bent Bone Dysplasia with Distinctive Clavicles and Angel-shaped Phalanges

Journal

AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 170, Issue 10, Pages 2652-2661

Publisher

WILEY-BLACKWELL
DOI: 10.1002/ajmg.a.37772

Keywords

skeletal dysplasia; FGFR2; craniosynostosis; bent bone dysplasia

Funding

  1. National Institutes of Health [RO1 AR066124, R01 AR062651, R01 DE025222, PO1 HD070394]
  2. March of Dimes
  3. Joseph Drown Foundation
  4. Orthopaedic Institute for Children
  5. March of Dimes Gene Discovery and Translation Research [6-FY15-233]

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Bent Bone Dysplasia-FGFR2 type is a relatively recently described bent bone phenotype with diagnostic clinical, radiographic, and molecular characteristics. Here we report on 11 individuals, including the original four patients plus seven new individuals with three longer-term survivors. The prenatal phenotype included stillbirth, bending of the femora, and a high incidence of polyhydramnios, prematurity, and perinatal death in three of 11 patients in the series. The survivors presented with characteristic radiographic findings that were observed among those with lethality, including bent bones, distinctive (moustache-shaped) small clavicles, angel-shaped metacarpals and phalanges, poor mineralization of the calvarium, and craniosynostosis. Craniofacial abnormalities, hirsutism, hepatic abnormalities, and genitourinary abnormalities were noted as well. Longer-term survivors all needed ventilator support. Heterozygosity for mutations in the gene that encodes Fibroblast Growth Factor Receptor 2 (FGFR2) was identified in the nine individuals with available DNA. Description of these patients expands the prenatal and postnatal findings of Bent Bone Dysplasia-FGFR2 type and adds to the phenotypic spectrum among all FGFR2 disorders. (c) 2016 Wiley Periodicals, Inc.

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