Literature DB >> 17994231

Cushing proximal symphalangism and the NOG and GDF5 genes.

Sara K Plett1, Walter E Berdon, Robert A Cowles, Rahmi Oklu, John B Campbell.   

Abstract

Proximal symphalangism (SYM1) is an autosomal-dominant developmental disorder of joint fusion. This disorder is best known from famous historical descriptions of two large kindred: Cushing's description in 1916 of the "straight-fingered" Brown family of Virginia and Drinkwater's description in 1917 of the British Talbot family of noble blood, descended from the English war hero John Talbot, the first Earl of Shrewsbury (1388-1453). Recent genetic studies link this phenotype to expression of abnormal genes at future joint sites: too little expression of NOG, a growth antagonist, or overexpression of GDF5, a growth agonist, results in cartilage overgrowth and bony fusion. This review unites in depth the first historical accounts of SYM1 with a clinical description and reviews the current understanding of the molecular mechanism underlying what is likely the oldest dominant trait ever studied.

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Year:  2007        PMID: 17994231     DOI: 10.1007/s00247-007-0675-y

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  8 in total

1.  Hereditary Anchylosis of the Proximal Phalan-Geal Joints (Symphalangism).

Authors:  H Cushing
Journal:  Genetics       Date:  1916-01       Impact factor: 4.562

2.  Phalangeal Anarthrosis (Synostosis, Ankylosis) transmitted through Fourteen Generations.

Authors:  H Drinkwater
Journal:  Proc R Soc Med       Date:  1917

3.  Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton.

Authors:  L J Brunet; J A McMahon; A P McMahon; R M Harland
Journal:  Science       Date:  1998-05-29       Impact factor: 47.728

4.  [Multiple synostosis disease].

Authors:  P Maroteaux; J P Bouvet; M L Briard
Journal:  Nouv Presse Med       Date:  1972-12-16

5.  Symphalangism and tarsal coalitions: a hereditary syndrome. A report on two families.

Authors:  G W Geelhoed; J V Neel; R T Davidson
Journal:  J Bone Joint Surg Br       Date:  1969-05

6.  Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis.

Authors:  Y Gong; D Krakow; J Marcelino; D Wilkin; D Chitayat; R Babul-Hirji; L Hudgins; C W Cremers; F P Cremers; H G Brunner; K Reinker; D L Rimoin; D H Cohn; F R Goodman; W Reardon; M Patton; C A Francomano; M L Warman
Journal:  Nat Genet       Date:  1999-03       Impact factor: 38.330

7.  The Talbot fingers: a study in symphalangism.

Authors:  S G Elkington; R G Huntsman
Journal:  Br Med J       Date:  1967-02-18

8.  Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2.

Authors:  Petra Seemann; Raphaela Schwappacher; Klaus W Kjaer; Deborah Krakow; Katarina Lehmann; Katherine Dawson; Sigmar Stricker; Jens Pohl; Frank Plöger; Eike Staub; Joachim Nickel; Walter Sebald; Petra Knaus; Stefan Mundlos
Journal:  J Clin Invest       Date:  2005-08-25       Impact factor: 14.808

  8 in total
  6 in total

1.  Recurrent missense mutation of GDF5 (p.R438L) causes proximal symphalangism in a British family.

Authors:  Andreas Leonidou; Melita Irving; Simon Holden; Marcos Katchburian
Journal:  World J Orthop       Date:  2016-12-18

2.  DNA hypermethylation of GDF5 in developmental dysplasia of the hip (DDH).

Authors:  Taghi Baghdadi; Mohammad Nejadhosseinian; Reza Shirkoohi; Reza Mostafavi Tabatabaee; Seyed S Tamehri; Mojtaba Saffari; S M Javad Mortazavi
Journal:  Mol Genet Genomic Med       Date:  2019-07-23       Impact factor: 2.183

3.  Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling.

Authors:  Cong Ma; Lv Liu; Fang-Na Wang; Hai-Shen Tian; Yan Luo; Rong Yu; Liang-Liang Fan; Ya-Li Li
Journal:  BMC Med Genet       Date:  2019-11-06       Impact factor: 2.103

4.  Proximal interphalangeal-level fracture in patient with symphalangism.

Authors:  Tommy Pan; Don Hoang; Alexander Payatakes
Journal:  Case Reports Plast Surg Hand Surg       Date:  2022-09-28

5.  Knock-in human GDF5 proregion L373R mutation as a mouse model for proximal symphalangism.

Authors:  Xinxin Zhang; Xuesha Xing; Xing Liu; Yu Hu; Shengqiang Qu; Heyi Wang; Yang Luo
Journal:  Oncotarget       Date:  2017-12-08

Review 6.  Interstitial duplication of 20q11.22q13.11: A case report and review of literature.

Authors:  Logan Goetzinger; Rachel D Starks; Kyle Dillahunt; Heather Major; Jaime M Nagy; Alpa Sidhu
Journal:  Mol Genet Genomic Med       Date:  2021-07-16       Impact factor: 2.473

  6 in total

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