Literature DB >> 7546453

"C" trigonocephaly syndrome with diaphragmnatic hernia.

M C Addor1, D Stefanutti, F Farron, P Meinecke, D Lacombe, J Sarlangue, G Prescia, D F Schorderet.   

Abstract

We report on a 6-year-old girl with C-trigonocephaly syndrome and diaphragmatic hernia. She is severely mentally retarded and shows the characteristic findings of this syndrome, including trigonocephaly, unusual facial features, especially intra-oral anomalies, low set and dysplastic ears, cardiac anomaly and neonatal hypotonia. Following our presentation at the 5th European meeting of dysmorphology in Strasbourg, P. Meinecke brought to our attention a case of C-trigonocephaly who died in the neonatal period from complications of a diaphragmatic hernia. Another case of C-trigonocephaly without diaphragmatic hernia was communicated to us by D. Lacombe. We report these three observations and present a review of 26 alleged cases.

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Mesh:

Year:  1995        PMID: 7546453

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  3 in total

1.  Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance.

Authors:  Bianca Russell; Jennifer J Johnston; Leslie G Biesecker; Nancy Kramer; Angela Pickart; William Rhead; Wen-Hann Tan; Catherine A Brownstein; L Kate Clarkson; Amy Dobson; Avi Z Rosenberg; Samantha A Schrier Vergano; Benjamin M Helm; Rachel E Harrison; John M Graham
Journal:  Am J Med Genet A       Date:  2015-04-29       Impact factor: 2.802

Review 2.  Bohring-Opitz (Oberklaid-Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis.

Authors:  Rob Hastings; Jan-Maarten Cobben; Gabriele Gillessen-Kaesbach; Judith Goodship; Hanne Hove; Susanne Kjaergaard; Helena Kemp; Helen Kingston; Peter Lunt; Sahar Mansour; Ruth McGowan; Kay Metcalfe; Catherine Murdoch-Davis; Mary Ray; Marlène Rio; Sarah Smithson; John Tolmie; Peter Turnpenny; Bregje van Bon; Dagmar Wieczorek; Ruth Newbury-Ecob
Journal:  Eur J Hum Genet       Date:  2011-02-02       Impact factor: 4.246

Review 3.  Genetic causes of congenital diaphragmatic hernia.

Authors:  Julia Wynn; Lan Yu; Wendy K Chung
Journal:  Semin Fetal Neonatal Med       Date:  2014-10-28       Impact factor: 3.926

  3 in total

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