Literature DB >> 7802004

Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndrome.

P Edery1, Y Manach, M Le Merrer, M Till, A Vignal, S Lyonnet, A Munnich.   

Abstract

The Treacher Collins-Franceschetti syndrome (TCOF) or mandibulofacial dysostosis (MFD) is an autosomal dominant disorder characterized by craniofacial abnormalities and hearing loss. A refined genetic linkage map of the TCOF locus was established in 8 independent families, using 12 microsatellite DNA markers of the distal 5q. Positive lod score values were obtained for all markers with a maximum at the D5S413 locus (Zmax = 3.79 at theta = 0%). Multipoint linkage analysis and haplotype analysis supported the location of the gene between loci D5S434 and D5S412. These results are consistent with previous linkage analyses [Dixon et al.: Am J Hum Genet 49:17-22, 1991, Am J Hum Genet 52:907-914, 1993; Jabs et al.: Genomics 11:193-198, 1991, Genomics 18:7-13, 1993] and provide further evidence of genetic homogeneity in this syndrome.

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Year:  1994        PMID: 7802004     DOI: 10.1002/ajmg.1320520210

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


  6 in total

Review 1.  Treacher Collins syndrome: clinical implications for the paediatrician--a new mutation in a severely affected newborn and comparison with three further patients with the same mutation, and review of the literature.

Authors:  Jan-Ulrich Schlump; Anja Stein; Ute Hehr; Tanja Karen; Claudia Möller-Hartmann; Nursel H Elcioglu; Nadja Bogdanova; Hartmut Fritz Woike; Dietmar R Lohmann; Ursula Felderhoff-Mueser; Annette Linz; Dagmar Wieczorek
Journal:  Eur J Pediatr       Date:  2012-06-23       Impact factor: 3.183

Review 2.  Treacher Collins syndrome.

Authors:  M J Dixon
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

3.  Human and murine PTX1/Ptx1 gene maps to the region for Treacher Collins syndrome.

Authors:  M J Crawford; C Lanctôt; J J Tremblay; N Jenkins; D Gilbert; N Copeland; B Beatty; J Drouin
Journal:  Mamm Genome       Date:  1997       Impact factor: 2.957

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

Authors:  S J Edwards; A Fowlie; M P Cust; D T Liu; I D Young; M J Dixon
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

Review 5.  Dysregulation of RNA polymerase I transcription during disease.

Authors:  K M Hannan; E Sanij; L I Rothblum; R D Hannan; R B Pearson
Journal:  Biochim Biophys Acta       Date:  2012-11-12

6.  Treacher Collins Syndrome with choanal atresia: a case report and review of disease features.

Authors:  Eduardo C Andrade; Vanier S Júnior; Ana L S Didoni; Priscila Z Freitas; Araken F Carneiro; Fabiana R Yoshimoto
Journal:  Braz J Otorhinolaryngol       Date:  2006-01-02
  6 in total

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