Literature DB >> 1519658

Beare-Stevenson cutis gyrata syndrome.

B D Hall1, R G Cadle, M Golabi, C A Morris, M M Cohen.   

Abstract

Beare-Stevenson cutis gyrata syndrome consists of skin furrows of corrugated appearance, acanthosis nigricans, craniofacial anomalies, particularly craniosynostosis and ear defects, anogenital anomalies, skin tags, and prominent umbilical stump. Four cases of this striking syndrome are reported. Together with two previously reported cases, the syndrome is delineated from the six known cases. Cutis gyrata variably affects the scalp, forehead, face, preauricular area, neck, trunk, hands, and feet. Craniosynostosis is present in four cases, with cloverleaf skull in three of these. Intrauterine growth has been normal in all cases. Performance and life expectation appear to be related to the presence or absence of cloverleaf skull. All cases observed to date have been sporadic. Increased paternal age suggests the possibility of an autosomal dominant mutation.

Entities:  

Mesh:

Year:  1992        PMID: 1519658     DOI: 10.1002/ajmg.1320440120

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  12 in total

Review 1.  Syndromic craniosynostosis, fibroblast growth factor receptor 2 (FGFR2) mutations, and sacrococcygeal eversion presenting as human tails.

Authors:  C Corbett Wilkinson; David K Manchester; Robert F Keating; Lawrence L Ketch; Ken R Winston
Journal:  Childs Nerv Syst       Date:  2012-06-04       Impact factor: 1.475

Review 2.  Choanal Atresia and Craniosynostosis: Development and Disease.

Authors:  Kate M Lesciotto; Yann Heuzé; Ethylin Wang Jabs; Joseph M Bernstein; Joan T Richtsmeier
Journal:  Plast Reconstr Surg       Date:  2018-01       Impact factor: 4.730

3.  Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongation.

Authors:  Kenneth E White; Jose M Cabral; Siobhan I Davis; Tonya Fishburn; Wayne E Evans; Shoji Ichikawa; Joanna Fields; Xijie Yu; Nick J Shaw; Neil J McLellan; Carole McKeown; David Fitzpatrick; Kai Yu; David M Ornitz; Michael J Econs
Journal:  Am J Hum Genet       Date:  2004-12-28       Impact factor: 11.025

4.  Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndrome.

Authors:  Anne Slavotinek; Howard Crawford; Mahin Golabi; Cathy Tao; Hazel Perry; Sneha Oberoi; Karin Vargervik; Michael Friez
Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802

5.  p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice.

Authors:  Yingli Wang; Xueyan Zhou; Kurun Oberoi; Robert Phelps; Ross Couwenhoven; Miao Sun; Amélie Rezza; Greg Holmes; Christopher J Percival; Jenna Friedenthal; Pavel Krejci; Joan T Richtsmeier; David L Huso; Michael Rendl; Ethylin Wang Jabs
Journal:  J Clin Invest       Date:  2012-05-15       Impact factor: 14.808

Review 6.  Genetic insights into the mechanisms of Fgf signaling.

Authors:  J Richard Brewer; Pierre Mazot; Philippe Soriano
Journal:  Genes Dev       Date:  2016-04-01       Impact factor: 11.361

Review 7.  Fibroblast Growth Factor Receptor 2 (FGFR2) Mutation Related Syndromic Craniosynostosis.

Authors:  Saïd C Azoury; Sashank Reddy; Vivek Shukla; Chu-Xia Deng
Journal:  Int J Biol Sci       Date:  2017-11-02       Impact factor: 6.580

8.  The first Korean case of Beare-Stevenson syndrome with a Tyr375Cys mutation in the fibroblast growth factor receptor 2 gene.

Authors:  So-Hee Eun; Ki Ssu Ha; Bo-Kyung Je; Eung Seok Lee; Byung Min Choi; Jung Hwa Lee; Baik-Lin Eun; Kee Hwan Yoo
Journal:  J Korean Med Sci       Date:  2007-04       Impact factor: 2.153

9.  A Case of Beare-Stevenson Syndrome with Unusual Manifestations.

Authors:  Nitin Ron; Samuel Leung; Erin Carney; Alexis Gerber; Karen Laurie David
Journal:  Am J Case Rep       Date:  2016-04-15

10.  Report of a Father With Congenital Bilateral Absence of the Vas Deferens Fathering a Child With Beare-Stevenson Syndrome.

Authors:  Leonardo C Ferreira; José H Dantas Junior
Journal:  Front Genet       Date:  2020-02-25       Impact factor: 4.599

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.