Literature DB >> 18461363

Clinical and radiological findings in Schinzel-Giedion syndrome.

Mudaffer Al-Mudaffer1, Christine Oley, Sue Price, Ian Hayes, Alison Stewart, Christine M Hall, William Reardon.   

Abstract

The absence of a definitive genetic test for the autosomal recessive condition Schinzel-Giedion syndrome is a significant handicap to the recognition of this disorder. Radiological features have been an important aspect of many of the published cases. In a series of six cases, we now establish a consistency among many of the radiological features in affected cases which will be an important diagnostic aid in identifying future cases. This is confirmed by reference to an extensive review of previously published instances of the syndrome. Moreover, the clinical data, including previously unpublished photographs, which we detail from our patients will assist in enhanced diagnosis in the future.

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Year:  2008        PMID: 18461363     DOI: 10.1007/s00431-008-0683-4

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  30 in total

1.  A Schinzel-Giedion-like syndrome--a milder version or a separate condition?

Authors:  Shelagh Joss; John C S Dean
Journal:  Clin Dysmorphol       Date:  2002-10       Impact factor: 0.816

2.  Schinzel-Giedion syndrome and alacrima: a case first described in 1996.

Authors:  Sylvie Manouvrier-Hanu
Journal:  Am J Med Genet A       Date:  2003-07-15       Impact factor: 2.802

Review 3.  The Schinzel-Giedion syndrome. A case report and review of the literature.

Authors:  M Pul; N Yilmaz; B Komsuoglu
Journal:  Clin Pediatr (Phila)       Date:  1990-04       Impact factor: 1.168

4.  A Croatian case of the Schinzel-Giedion syndrome.

Authors:  V Culić; B Resic; J W Oorthuys; W C Overweg-Plandsoen; R C Hennekam
Journal:  Genet Couns       Date:  1996

5.  A further case of a new syndrome including midface retraction, hypertrichosis, and skeletal anomalies.

Authors:  D Donnai; R Harris
Journal:  J Med Genet       Date:  1979-12       Impact factor: 6.318

6.  Schinzel-Giedion syndrome.

Authors:  S Alavi; A Kher; B A Bharucha
Journal:  Indian Pediatr       Date:  1994-09       Impact factor: 1.411

7.  Schinzel-Giedion syndrome: evidence for a neurodegenerative process.

Authors:  A M Shah; M F Smith; P D Griffiths; O W Quarrell
Journal:  Am J Med Genet       Date:  1999-02-12

8.  Neurosonography and pathology in the Schinzel-Giedion syndrome.

Authors:  A C Maclennan; D Doyle; R M Simpson
Journal:  J Med Genet       Date:  1991-08       Impact factor: 6.318

9.  Schinzel-Giedion syndrome.

Authors:  A Verloes; D Moës; L Palumbo; C Elmer; A François; G Bricteux
Journal:  Eur J Pediatr       Date:  1993-05       Impact factor: 3.183

Review 10.  A patient with Schinzel-Giedion syndrome and a review of 20 patients.

Authors:  N Okamoto; M Takeuchi; H Kitajima; S Hosokawa
Journal:  Jpn J Hum Genet       Date:  1995-06
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  5 in total

Review 1.  Schinzel-Giedion syndrome: a novel case, review and revised diagnostic criteria.

Authors:  Wei-Liang Liu; Zhi-Xu He; Fang Li; Rong Ai; Hong-Wei Ma
Journal:  J Genet       Date:  2018-03       Impact factor: 1.166

2.  Distinct neurological features in a patient with Schinzel-Giedion syndrome caused by a recurrent SETBP1 mutation.

Authors:  Jung Min Ko; Byung Chan Lim; Ki Joong Kim; Yong Seung Hwang; Hye Won Ryu; Jung Ho Lee; Jon Su Kim; Jong-Hee Chae
Journal:  Childs Nerv Syst       Date:  2013-02-12       Impact factor: 1.475

3.  SETBP1 accumulation induces P53 inhibition and genotoxic stress in neural progenitors underlying neurodegeneration in Schinzel-Giedion syndrome.

Authors:  Federica Banfi; Alicia Rubio; Mattia Zaghi; Luca Massimino; Giulia Fagnocchi; Edoardo Bellini; Mirko Luoni; Cinzia Cancellieri; Anna Bagliani; Chiara Di Resta; Camilla Maffezzini; Angelo Ianielli; Maurizio Ferrari; Rocco Piazza; Luca Mologni; Vania Broccoli; Alessandro Sessa
Journal:  Nat Commun       Date:  2021-06-30       Impact factor: 14.919

4.  Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.

Authors:  Rocio Acuna-Hidalgo; Pelagia Deriziotis; Marloes Steehouwer; Christian Gilissen; Sarah A Graham; Sipko van Dam; Julie Hoover-Fong; Aida B Telegrafi; Anne Destree; Robert Smigiel; Lindsday A Lambie; Hülya Kayserili; Umut Altunoglu; Elisabetta Lapi; Maria Luisa Uzielli; Mariana Aracena; Banu G Nur; Ercan Mihci; Lilia M A Moreira; Viviane Borges Ferreira; Dafne D G Horovitz; Katia M da Rocha; Aleksandra Jezela-Stanek; Alice S Brooks; Heiko Reutter; Julie S Cohen; Ali Fatemi; Martin Smitka; Theresa A Grebe; Nataliya Di Donato; Charu Deshpande; Anthony Vandersteen; Charles Marques Lourenço; Andreas Dufke; Eva Rossier; Gwenaelle Andre; Alessandra Baumer; Careni Spencer; Julie McGaughran; Lude Franke; Joris A Veltman; Bert B A De Vries; Albert Schinzel; Simon E Fisher; Alexander Hoischen; Bregje W van Bon
Journal:  PLoS Genet       Date:  2017-03-27       Impact factor: 5.917

5.  Whole-genome sequencing combined RNA-sequencing analysis of patients with mutations in SET binding protein 1.

Authors:  Li Liu; Xiaoshu Feng; Sihan Liu; Yanqiu Zhou; Xiaojing Dong; Hong Yao; Bo Tan
Journal:  Front Neurosci       Date:  2022-09-07       Impact factor: 5.152

  5 in total

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