Literature DB >> 8818950

Prenatal diagnosis in Treacher Collins syndrome using combined linkage analysis and ultrasound imaging.

S J Edwards1, A Fowlie, M P Cust, D T Liu, I D Young, M J Dixon.   

Abstract

Treacher Collins syndrome is an autosomal dominant disorder of facial development, the features of which include conductive hearing loss and cleft palate. In the current investigation, linkage analysis has been used to make first trimester diagnostic predictions in a pregnancy at high risk of producing an affected child. The results of this analysis predicted that the child would be affected. As predictions of the severity of the disease were not possible, the pregnancy was also assessed by ultrasound imaging. This confirmed the affected diagnosis and predicted that the child would be severely affected.

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Year:  1996        PMID: 8818950      PMCID: PMC1050672          DOI: 10.1136/jmg.33.7.603

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  20 in total

1.  Dinucleotide repeat polymorphism at the human c-fms protooncogene for the CFS-1 receptor (CFS1R).

Authors:  M H Polymeropoulos; H Xiao; D S Rath; C R Merril
Journal:  Nucleic Acids Res       Date:  1991-03-11       Impact factor: 16.971

2.  Mapping the Treacher Collins syndrome locus to 5q31.3----q33.3.

Authors:  E W Jabs; X Li; C A Coss; E W Taylor; D A Meyers; J L Weber
Journal:  Genomics       Date:  1991-09       Impact factor: 5.736

3.  Transcriptional map of the Treacher Collins candidate gene region.

Authors:  S K Loftus; J Dixon; K Koprivnikar; M J Dixon; J J Wasmuth
Journal:  Genome Res       Date:  1996-01       Impact factor: 9.043

4.  Chromosomal deletion 4p15.32----p14 in a Treacher Collins syndrome patient: exclusion of the disease locus from and mapping of anonymous DNA sequences to this region.

Authors:  E W Jabs; C A Coss; S J Hayflick; T E Whitmore; R M Pauli; S J Kirkpatrick; D A Meyers; R Goldberg; D W Day; K N Rosenbaum
Journal:  Genomics       Date:  1991-09       Impact factor: 5.736

5.  Association of Treacher Collins syndrome and translocation 6p21.31/16p13.11: exclusion of the locus from these candidate regions.

Authors:  M J Dixon; E Haan; E Baker; D David; N McKenzie; R Williamson; J Mulley; M Farrall; D Callen
Journal:  Am J Hum Genet       Date:  1991-02       Impact factor: 11.025

Review 6.  Fetoscopy and fetal tissue sampling.

Authors:  C H Rodeck; K H Nicolaides
Journal:  Br Med Bull       Date:  1983-10       Impact factor: 4.291

7.  Prenatal diagnosis of mandibulofacial dysostosis.

Authors:  K H Nicolaides; D Johansson; D Donnai; C H Rodeck
Journal:  Prenat Diagn       Date:  1984 May-Jun       Impact factor: 3.050

8.  Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q.

Authors:  S G Ryan; M J Dixon; M A Nigro; K A Kelts; O N Markand; J C Terry; R Shiang; J J Wasmuth; P O'Connell
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

9.  The ear deformities in mandibulofacial dysostosis (Treacher Collins syndrome).

Authors:  P D Phelps; D Poswillo; G A Lloyd
Journal:  Clin Otolaryngol Allied Sci       Date:  1981-02

10.  Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms.

Authors:  J L Weber
Journal:  Genomics       Date:  1990-08       Impact factor: 5.736

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  11 in total

1.  Treacher Collins syndrome with novel ophthalmic findings and visceral anomalies.

Authors:  J L Prenner; G Binenbaum; D F Carpentieri; S M Goldstein; R S Douglas; E Ruchelli; J A Katowitz; R W Hertle
Journal:  Br J Ophthalmol       Date:  2002-04       Impact factor: 4.638

Review 2.  Craniofacial birth defects: The role of neural crest cells in the etiology and pathogenesis of Treacher Collins syndrome and the potential for prevention.

Authors:  Paul A Trainor
Journal:  Am J Med Genet A       Date:  2010-08-23       Impact factor: 2.802

Review 3.  Facial dysostoses: Etiology, pathogenesis and management.

Authors:  Paul A Trainor; Brian T Andrews
Journal:  Am J Med Genet C Semin Med Genet       Date:  2013-10-04       Impact factor: 3.908

4.  The mutational spectrum in Treacher Collins syndrome reveals a predominance of mutations that create a premature-termination codon.

Authors:  S J Edwards; A J Gladwin; M J Dixon
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

Review 5.  Rare syndromes of the head and face: mandibulofacial and acrofacial dysostoses.

Authors:  Karla Terrazas; Jill Dixon; Paul A Trainor; Michael J Dixon
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2017-02-10       Impact factor: 5.814

Review 6.  Face off against ROS: Tcof1/Treacle safeguards neuroepithelial cells and progenitor neural crest cells from oxidative stress during craniofacial development.

Authors:  Daisuke Sakai; Paul A Trainor
Journal:  Dev Growth Differ       Date:  2016-08-02       Impact factor: 2.053

7.  First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome.

Authors:  J Beygo; K Buiting; S Seland; H-J Lüdecke; U Hehr; C Lich; B Prager; D R Lohmann; D Wieczorek
Journal:  Mol Syndromol       Date:  2012-01-26

8.  Treacher Collins syndrome: etiology, pathogenesis and prevention.

Authors:  Paul A Trainor; Jill Dixon; Michael J Dixon
Journal:  Eur J Hum Genet       Date:  2008-12-24       Impact factor: 4.246

Review 9.  From Bench to Bedside and Back: Improving Diagnosis and Treatment of Craniofacial Malformations Utilizing Animal Models.

Authors:  Alice F Goodwin; Rebecca Kim; Jeffrey O Bush; Ophir D Klein
Journal:  Curr Top Dev Biol       Date:  2015-10-06       Impact factor: 4.897

Review 10.  Diabetes, Oxidative Stress, and DNA Damage Modulate Cranial Neural Crest Cell Development and the Phenotype Variability of Craniofacial Disorders.

Authors:  Sharien Fitriasari; Paul A Trainor
Journal:  Front Cell Dev Biol       Date:  2021-05-20
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