Mandibulofacial dysostosis in Hutterite sibs: a possible recessive trait
- PMID: 4061487
- DOI: 10.1002/ajmg.1320220308
Mandibulofacial dysostosis in Hutterite sibs: a possible recessive trait
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%.
Similar articles
-
Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance.Am J Med Genet. 1993 Jul 1;46(6):659-64. doi: 10.1002/ajmg.1320460611. Am J Med Genet. 1993. PMID: 8362908
-
Melnick-Needles syndrome: indication for an autosomal recessive form.Am J Med Genet. 1982 Dec;13(4):469-77. doi: 10.1002/ajmg.1320130418. Am J Med Genet. 1982. PMID: 7158646
-
Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerleut Hutterite family from Montana.Am J Med Genet. 1985 Nov;22(3):521-9. doi: 10.1002/ajmg.1320220310. Am J Med Genet. 1985. PMID: 4061488
-
Acrofacial dysostoses: review and report of a previously undescribed condition: the autosomal or X-linked dominant Catania form of acrofacial dysostosis.Am J Med Genet. 1993 Oct 1;47(5):660-78. doi: 10.1002/ajmg.1320470517. Am J Med Genet. 1993. PMID: 8266994 Review.
-
Gonadal mosaicism in pseudoachondroplasia.Am J Med Genet. 1987 Sep;28(1):143-51. doi: 10.1002/ajmg.1320280121. Am J Med Genet. 1987. PMID: 3314506 Review.
Cited by
-
Common mechanisms in development and disease: BMP signaling in craniofacial development.Cytokine Growth Factor Rev. 2016 Feb;27:129-39. doi: 10.1016/j.cytogfr.2015.11.004. Epub 2015 Nov 24. Cytokine Growth Factor Rev. 2016. PMID: 26747371 Free PMC article. Review.
-
The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis.Genes (Basel). 2018 May 16;9(5):255. doi: 10.3390/genes9050255. Genes (Basel). 2018. PMID: 29772684 Free PMC article. Review.
-
Possible germline mosaicism in a pedigree with Treacher Collins syndrome: A case report and brief review.Sci Prog. 2024 Apr-Jun;107(2):368504241242278. doi: 10.1177/00368504241242278. Sci Prog. 2024. PMID: 38629201 Free PMC article. Review.
-
Mutation screening of Chinese Treacher Collins syndrome patients identified novel TCOF1 mutations.Mol Genet Genomics. 2018 Apr;293(2):569-577. doi: 10.1007/s00438-017-1384-3. Epub 2017 Dec 11. Mol Genet Genomics. 2018. PMID: 29230583
-
Mutational Analysis of TCOF1, GSC, and HOXA2 in Patients With Treacher Collins Syndrome.J Craniofac Surg. 2016 Sep;27(6):e583-6. doi: 10.1097/SCS.0000000000002934. J Craniofac Surg. 2016. PMID: 27526242 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources