Literature DB >> 11546827

Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location.

C A Boucher1, C A Sargent, T Ogata, N A Affara.   

Abstract

BACKGROUND: Turner syndrome is characterised by a 45,X karyotype and a variety of skeletal, lymphoedemic, and gonadal anomalies. Genes involved in the Turner phenotype are thought to be X/Y homologous with the X genes escaping X inactivation. Haploinsufficiency of the SHOX gene has been reported to cause the short stature seen in Turner syndrome patients. More recently, mutations of this gene have been shown to be associated with other skeletal abnormalities, suggesting that haploinsufficiency of SHOX causes all the Turner skeletal anomalies. No such gene has yet been identified for the lymphoedemic features.
METHODS: Fluorescence in situ hybridisation (FISH) analysis with PAC clones on nine patients with partially deleted X chromosomes was performed. RESULTS/DISCUSSION: The Turner syndrome stigmata for each patient are described and correlation between the breakpoint and the phenotype discussed. A lymphoedema critical region in Xp11.4 is proposed and its gene content discussed with respect to that in the previously reported Yp11.2 lymphoedema critical region.

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Year:  2001        PMID: 11546827      PMCID: PMC1734929          DOI: 10.1136/jmg.38.9.591

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  28 in total

1.  Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: a clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmata.

Authors:  T Hasegawa; T Ogata; Y Hasegawa; M Honda; T Nagai; Y Fukushima; Y Nakahori; N Matsuo
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

2.  A set of ninety-seven overlapping yeast artificial chromosome clones spanning the human Y chromosome euchromatin.

Authors:  M H Jones; O S Khwaja; H Briggs; B Lambson; P M Davey; J Chalmers; C Y Zhou; E M Walker; Y Zhang; C Todd
Journal:  Genomics       Date:  1994-11-15       Impact factor: 5.736

3.  A study of females with deletions of the short arm of the X chromosome.

Authors:  R S James; B Coppin; P Dalton; N R Dennis; C Mitchell; A J Sharp; D H Skuse; N S Thomas; P A Jacobs
Journal:  Hum Genet       Date:  1998-05       Impact factor: 4.132

4.  Del (X)(p21.2) in a mother and two daughters with variable ovarian function.

Authors:  A R Zinn; B Ouyang; J L Ross; S Varma; M Bourgeois; V Tonk
Journal:  Clin Genet       Date:  1997-10       Impact factor: 4.438

5.  The Drosophila developmental gene fat facets has a human homologue in Xp11.4 which escapes X-inactivation and has related sequences on Yq11.2.

Authors:  M H Jones; R A Furlong; H Burkin; I J Chalmers; G M Brown; O Khwaja; N A Affara
Journal:  Hum Mol Genet       Date:  1996-11       Impact factor: 6.150

6.  Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis.

Authors:  D J Shears; H J Vassal; F R Goodman; R W Palmer; W Reardon; A Superti-Furga; P J Scambler; R M Winter
Journal:  Nat Genet       Date:  1998-05       Impact factor: 38.330

7.  Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome.

Authors:  E Rao; B Weiss; M Fukami; A Rump; B Niesler; A Mertz; K Muroya; G Binder; S Kirsch; M Winkelmann; G Nordsiek; U Heinrich; M H Breuning; M B Ranke; A Rosenthal; T Ogata; G A Rappold
Journal:  Nat Genet       Date:  1997-05       Impact factor: 38.330

8.  Vascular endothelial growth factor D (VEGF-D) is a ligand for the tyrosine kinases VEGF receptor 2 (Flk1) and VEGF receptor 3 (Flt4).

Authors:  M G Achen; M Jeltsch; E Kukk; T Mäkinen; A Vitali; A F Wilks; K Alitalo; S A Stacker
Journal:  Proc Natl Acad Sci U S A       Date:  1998-01-20       Impact factor: 11.205

9.  Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.

Authors:  A R Zinn; V S Tonk; Z Chen; W L Flejter; H A Gardner; R Guerra; H Kushner; S Schwartz; V P Sybert; D L Van Dyke; J L Ross
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

Review 10.  Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.

Authors:  T Ogata; N Matsuo
Journal:  Hum Genet       Date:  1995-06       Impact factor: 4.132

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  12 in total

1.  A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions.

Authors:  K L Lachlan; S Youings; T Costa; P A Jacobs; N S Thomas
Journal:  Hum Genet       Date:  2005-11-08       Impact factor: 4.132

Review 2.  Optimising management in Turner syndrome: from infancy to adult transfer.

Authors:  M D C Donaldson; E J Gault; K W Tan; D B Dunger
Journal:  Arch Dis Child       Date:  2006-06       Impact factor: 3.791

3.  Altered immune response in mice deficient for the G protein-coupled receptor GPR34.

Authors:  Ines Liebscher; Uwe Müller; Daniel Teupser; Eva Engemaier; Kathrin M Y Engel; Lars Ritscher; Doreen Thor; Katrin Sangkuhl; Albert Ricken; Antje Wurm; Daniel Piehler; Sandra Schmutzler; Herbert Fuhrmann; Frank W Albert; Andreas Reichenbach; Joachim Thiery; Torsten Schöneberg; Angela Schulz
Journal:  J Biol Chem       Date:  2010-11-19       Impact factor: 5.157

4.  A five generation family with a novel mutation in FOXC2 and lymphedema worsening to hydrops in the youngest generation.

Authors:  Carole Sargent; Julien Bauer; Muhamed Khalil; Parker Filmore; Michael Bernas; Marlys Witte; M Peggy Pearson; Robert P Erickson
Journal:  Am J Med Genet A       Date:  2014-09-22       Impact factor: 2.802

5.  Vascular endothelial growth factor (VEGF) levels in short, GH treated children: a distinct pattern of VEGF-C in Noonan syndrome.

Authors:  S Fuchs; G Gat-Yablonski; B Shtaif; L Lazar; M Phillip; Y Lebenthal
Journal:  J Endocrinol Invest       Date:  2014-10-26       Impact factor: 4.256

6.  Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF).

Authors:  C R Quilter; A C Karcanias; M R Bagga; S Duncan; A Murray; G S Conway; C A Sargent; N A Affara
Journal:  Hum Reprod       Date:  2010-06-22       Impact factor: 6.918

7.  Cardiovascular anomalies in children and young adults with Ullrich-Turner syndrome the Erlangen experience.

Authors:  Thomas M K Völkl; Karin Degenhardt; Andreas Koch; Diemud Simm; Helmuth G Dörr; Helmut Singer
Journal:  Clin Cardiol       Date:  2005-02       Impact factor: 2.882

8.  Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia.

Authors:  Alexandre Irrthum; Koenraad Devriendt; David Chitayat; Gert Matthijs; Conrad Glade; Peter M Steijlen; Jean-Pierre Fryns; Maurice A M Van Steensel; Miikka Vikkula
Journal:  Am J Hum Genet       Date:  2003-05-08       Impact factor: 11.025

9.  Turner syndrome caused by rare complex structural abnormalities involving chromosome X.

Authors:  Niu Li; Li Zhao; Juan Li; Yu Ding; Yongnian Shen; Xiaodong Huang; Xiumin Wang; Jian Wang
Journal:  Exp Ther Med       Date:  2017-07-10       Impact factor: 2.447

Review 10.  The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review.

Authors:  Giles Atton; Kristiana Gordon; Glen Brice; Vaughan Keeley; Katie Riches; Pia Ostergaard; Peter Mortimer; Sahar Mansour
Journal:  Eur J Hum Genet       Date:  2015-03-25       Impact factor: 4.246

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