Literature DB >> 4061487

Mandibulofacial dysostosis in Hutterite sibs: a possible recessive trait.

R B Lowry, K Morgan, T M Holmes, P J Metcalf, G F Stauffer.   

Abstract

We report on two sisters with mandibulofacial dysostosis (MFD). Both parents were examined carefully by clinical, radiographic, audiologic, and cephalometric methods. Neither showed evidence of the MFD gene. Photographs of three grandparents and examination of one disclosed no evidence of MFD. The parents are from the Hutterite Brethren and are consanguineous. Examination of the literature on MFD disclosed a number of other families with affected sibs and apparently normal parents. These families raise the possibility of an autosomal recessive form of MFD or some other explanation such as germinal mosaicism, chromosome rearrangement, or delayed mutation. For our family, the recurrence risk is probably 25%, but since germinal mosaicism cannot be excluded, it could be as high as 50%.

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Year:  1985        PMID: 4061487     DOI: 10.1002/ajmg.1320220308

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

1.  Mutation screening of Chinese Treacher Collins syndrome patients identified novel TCOF1 mutations.

Authors:  Ying Chen; Luo Guo; Chen-Long Li; Jing Shan; Hai-Song Xu; Jie-Ying Li; Shan Sun; Shao-Juan Hao; Lei Jin; Gang Chai; Tian-Yu Zhang
Journal:  Mol Genet Genomics       Date:  2017-12-11       Impact factor: 3.291

2.  Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome.

Authors:  Johannes G Dauwerse; Jill Dixon; Saskia Seland; Claudia A L Ruivenkamp; Arie van Haeringen; Lies H Hoefsloot; Dorien J M Peters; Agnes Clement-de Boers; Cornelia Daumer-Haas; Robert Maiwald; Christiane Zweier; Bronwyn Kerr; Ana M Cobo; Joaquín F Toral; A Jeannette M Hoogeboom; Dietmar R Lohmann; Ute Hehr; Michael J Dixon; Martijn H Breuning; Dagmar Wieczorek
Journal:  Nat Genet       Date:  2010-12-05       Impact factor: 38.330

3.  Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts the HOXD gene cluster.

Authors:  David A Stevenson; Steven B Bleyl; Teresa Maxwell; Arthur R Brothman; Sarah T South
Journal:  Am J Med Genet A       Date:  2007-05-15       Impact factor: 2.802

Review 4.  Common mechanisms in development and disease: BMP signaling in craniofacial development.

Authors:  Daniel Graf; Zeba Malik; Satoru Hayano; Yuji Mishina
Journal:  Cytokine Growth Factor Rev       Date:  2015-11-24       Impact factor: 7.638

5.  Mutational Analysis of TCOF1, GSC, and HOXA2 in Patients With Treacher Collins Syndrome.

Authors:  Shaojuan Hao; Lei Jin; Huijun Wang; Chenlong Li; Fengyun Zheng; Duan Ma; Tianyu Zhang
Journal:  J Craniofac Surg       Date:  2016-09       Impact factor: 1.046

Review 6.  The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis.

Authors:  Meredith A Williams; Ariadne Letra
Journal:  Genes (Basel)       Date:  2018-05-16       Impact factor: 4.096

  6 in total

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