Literature DB >> 27240702

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

Deborah Krakow1,2,3,4, Daniel H Cohn5,6,7, William R Wilcox6,8, Grace J Noh9, Leslie J Raffel9, Anna Sarukhanov5, Margarita H Ivanova5, Moise Danielpour10, Dorothy K Grange11, Alison M Elliott12, Jonathan A Bernstein13, David L Rimoin, Amy E Merrill14, Ralph S Lachman6,15.   

Abstract

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.
© 2016 Wiley Periodicals, Inc. © 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  FGFR2; bent bone dysplasia; craniosynostosis; skeletal dysplasia

Mesh:

Substances:

Year:  2016        PMID: 27240702      PMCID: PMC5538138          DOI: 10.1002/ajmg.a.37772

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  14 in total

Review 1.  A new case of bent bone dysplasia--FGFR2 type and review of the literature.

Authors:  Morgane Stichelbout; Anne Dieux-Coeslier; Elodie Clouqueur; Corinne Collet; Florence Petit
Journal:  Am J Med Genet A       Date:  2015-11-17       Impact factor: 2.802

2.  Beare-Stevenson syndrome: two Dutch patients with cerebral abnormalities.

Authors:  Daniela Q C M Barge-Schaapveld; Alice S Brooks; Maarten H Lequin; Rosalinda van Spaendonk; R Jeroen Vermeulen; Jan Maarten Cobben
Journal:  Pediatr Neurol       Date:  2011-04       Impact factor: 3.372

3.  Apert syndrome with fused thalami.

Authors:  Kathrin Ludwig; Roberto Salmaso; Renzo Manara; Erich Cosmi; Maurizia Baldi; Massimo Rugge
Journal:  Fetal Pediatr Pathol       Date:  2012-03-23       Impact factor: 0.958

4.  Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling.

Authors:  Amy E Merrill; Anna Sarukhanov; Pavel Krejci; Brian Idoni; Natalia Camacho; Kristine D Estrada; Karen M Lyons; Hannah Deixler; Haynes Robinson; David Chitayat; Cynthia J Curry; Ralph S Lachman; William R Wilcox; Deborah Krakow
Journal:  Am J Hum Genet       Date:  2012-03-01       Impact factor: 11.025

5.  Membrane and integrative nuclear fibroblastic growth factor receptor (FGFR) regulation of FGF-23.

Authors:  Xiaobin Han; Zhousheng Xiao; L Darryl Quarles
Journal:  J Biol Chem       Date:  2015-03-09       Impact factor: 5.157

6.  Lacrimo-auriculo-dento-digital (LADD) syndrome.

Authors:  D W Hollister; S H Klein; H J de Jager; R S Lachman; D L Rimoin
Journal:  Birth Defects Orig Artic Ser       Date:  1974

7.  Mutations in different components of FGF signaling in LADD syndrome.

Authors:  Edyta Rohmann; Han G Brunner; Hülya Kayserili; Oya Uyguner; Gudrun Nürnberg; Erin D Lew; Angus Dobbie; Veraragavan P Eswarakumar; Abdullah Uzumcu; Melike Ulubil-Emeroglu; Jules G Leroy; Yun Li; Christian Becker; Kai Lehnerdt; Cor W R J Cremers; Memnune Yüksel-Apak; Peter Nürnberg; Christian Kubisch; Chriütian Kubisch; Joseph Schlessinger; Hans van Bokhoven; Bernd Wollnik
Journal:  Nat Genet       Date:  2006-02-26       Impact factor: 38.330

Review 8.  Altered FGF signalling in congenital craniofacial and skeletal disorders.

Authors:  Shahida Moosa; Bernd Wollnik
Journal:  Semin Cell Dev Biol       Date:  2015-12-11       Impact factor: 7.727

9.  Lacrimo-auriculo-dento-digital syndrome is caused by reduced activity of the fibroblast growth factor 10 (FGF10)-FGF receptor 2 signaling pathway.

Authors:  Imad Shams; Edyta Rohmann; Veraragavan P Eswarakumar; Erin D Lew; Satoru Yuzawa; Bernd Wollnik; Joseph Schlessinger; Irit Lax
Journal:  Mol Cell Biol       Date:  2007-08-06       Impact factor: 4.272

10.  Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

Authors:  Roman Hossein Khonsari; Anne-Lise Delezoide; Wenfei Kang; Jean M Hébert; Bettina Bessières; Valérie Bodiguel; Catherine Collet; Laurence Legeai-Mallet; Paul T Sharpe; Catherine Fallet-Bianco
Journal:  Am J Med Genet A       Date:  2012-09-17       Impact factor: 2.802

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  2 in total

Review 1.  Nuclear Fibroblast Growth Factor Receptor Signaling in Skeletal Development and Disease.

Authors:  Creighton T Tuzon; Diana Rigueur; Amy E Merrill
Journal:  Curr Osteoporos Rep       Date:  2019-06       Impact factor: 5.096

Review 2.  Clinical genetics of craniosynostosis.

Authors:  Andrew O M Wilkie; David Johnson; Steven A Wall
Journal:  Curr Opin Pediatr       Date:  2017-12       Impact factor: 2.856

  2 in total

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