Literature DB >> 18259761

Mowat--Wilson syndrome: the clinical report with the novel mutation in ZFHX1B (exon 8: c.2372del C; p.T791fsX816).

Antun Sasso1, Ela Paucić-Kirincić, Silvija Kamber-Makek, Nada Sindicić, S Brajnović-Zaputović, Bojana Brajenović-Milić.   

Abstract

INTRODUCTION: Mowat-Wilson syndrome is a congenital syndrome caused by a defect of the transcriptional repressor ZFHX1B (SIP1) gene on the chromosome 2q22-q23. The genotype-phenotype analysis confirmed that ZFHX1B deletions and mutations result in a recognizable facial dysmorphism with a multiple congenital anomaly and mental retardation. CASE REPORT: This report is about one new patient from Croatia with the typical phenotype. Molecular genetic studies showed the novel mutation in ZFHX1B (exon 8: c.2372del C; p.T791fsX816). This mutation has not been reported before. The literature is reviewed.
CONCLUSION: Mowat-Wilson syndrome is a newly described congenital syndrome and should be considered in any individual with characteristic facial features and mental retardation in associations with congenital malformations.

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Year:  2008        PMID: 18259761     DOI: 10.1007/s00381-007-0557-5

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  14 in total

1.  "Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene.

Authors:  Christiane Zweier; Beate Albrecht; Beate Mitulla; Rolf Behrens; Maike Beese; Gabriele Gillessen-Kaesbach; Hans-Dieter Rott; Anita Rauch
Journal:  Am J Med Genet       Date:  2002-03-15

Review 2.  Angelman syndrome: mimicking conditions and phenotypes.

Authors:  C A Williams; A Lossie; D Driscoll
Journal:  Am J Med Genet       Date:  2001-06-01

3.  Mowat-Wilson syndrome and mutation in the zinc finger homeo box 1B gene: a well defined clinical entity.

Authors:  P Cerruti Mainardi; G Pastore; C Zweier; A Rauch
Journal:  J Med Genet       Date:  2004-02       Impact factor: 6.318

4.  Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome.

Authors:  C Zweier; I K Temple; F Beemer; E Zackai; T Lerman-Sagie; B Weschke; C E Anderson; A Rauch
Journal:  J Med Genet       Date:  2003-08       Impact factor: 6.318

5.  Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22-q24.1.

Authors:  N Ishihara; K Yamada; Y Yamada; K Miura; J Kato; N Kuwabara; Y Hara; Y Kobayashi; K Hoshino; Y Nomura; M Mimaki; K Ohya; M Matsushima; H Nitta; K Tanaka; M Segawa; T Ohki; T Ezoe; T Kumagai; A Onuma; T Kuroda; M Yoneda; T Yamanaka; M Saeki; M Segawa; T Saji; M Nagaya; N Wakamatsu
Journal:  J Med Genet       Date:  2004-05       Impact factor: 6.318

6.  ZFHX1B mutations in patients with Mowat-Wilson syndrome.

Authors:  Florence Dastot-Le Moal; Meredith Wilson; David Mowat; Nathalie Collot; Florence Niel; Michel Goossens
Journal:  Hum Mutat       Date:  2007-04       Impact factor: 4.878

7.  A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotype.

Authors:  Wolfram Heinritz; Christiane Zweier; Ursula G Froster; Sibylle Strenge; Annegret Kujat; Steffen Syrbe; Anita Rauch; Volker Schuster
Journal:  Am J Med Genet A       Date:  2006-06-01       Impact factor: 2.802

8.  Recurrence of Mowat-Wilson syndrome in siblings with the same proven mutation.

Authors:  Julie McGaughran; Stephen Sinnott; Florence Dastot-Le Moal; Meredith Wilson; David Mowat; Bridget Sutton; Michel Goossens
Journal:  Am J Med Genet A       Date:  2005-09-01       Impact factor: 2.802

9.  Clinical features and management issues in Mowat-Wilson syndrome.

Authors:  Margaret P Adam; Susan Schelley; Renata Gallagher; April N Brady; Kimberly Barr; Bruce Blumberg; Joseph T C Shieh; John Graham; Anne Slavotinek; Madelena Martin; Kim Keppler-Noreuil; Andrea L Storm; Louanne Hudgins
Journal:  Am J Med Genet A       Date:  2006-12-15       Impact factor: 2.802

Review 10.  Hirschsprung disease, unusual face, mental retardation, epilepsy, and congenital heart disease: Goldberg-Shprintzen syndrome.

Authors:  H Tanaka; J Ito; K Cho; M Mikawa
Journal:  Pediatr Neurol       Date:  1993 Nov-Dec       Impact factor: 3.372

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  2 in total

Review 1.  Hirschsprung's disease in children with Mowat-Wilson syndrome.

Authors:  David Coyle; Prem Puri
Journal:  Pediatr Surg Int       Date:  2015-07-09       Impact factor: 1.827

2.  Clinical utility gene card for: Mowat-Wilson syndrome.

Authors:  Marcella Zollino; Livia Garavelli; Anita Rauch
Journal:  Eur J Hum Genet       Date:  2011-02-23       Impact factor: 4.246

  2 in total

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