Literature DB >> 24123981

Facial dysostoses: Etiology, pathogenesis and management.

Paul A Trainor, Brian T Andrews.   

Abstract

Approximately 1% of all live births exhibit a minor or major congenital anomaly. Of these approximately one-third display craniofacial abnormalities which are a significant cause of infant mortality and dramatically affect national health care budgets. To date, more than 700 distinct craniofacial syndromes have been described and in this review, we discuss the etiology, pathogenesis and management of facial dysostoses with a particular emphasis on Treacher Collins, Nager and Miller syndromes. As we continue to develop and improve medical and surgical care for the management of individual conditions, it is essential at the same time to better characterize their etiology and pathogenesis. Here we describe recent advances in our understanding of the development of facial dysostosis with a view towards early in utero identification and intervention which could minimize the manifestation of anomalies prior to birth. The ultimate management for any craniofacial anomaly however, would be prevention and we discuss this possibility in relation to facial dysostosis.
© 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  Miller syndrome; Nager syndrome; Treacher Collins syndrome; acrofacial dysotosis; facial dysostosis; mandibulofacial dysostosis; neural crest cells; ribosome biogenesis; spliceosome

Mesh:

Year:  2013        PMID: 24123981      PMCID: PMC3870197          DOI: 10.1002/ajmg.c.31375

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  66 in total

1.  Mandibulofacial dysostosis.

Authors:  J J STOVIN; J A LYON; R L CLEMMENS
Journal:  Radiology       Date:  1960-02       Impact factor: 11.105

2.  Total reconstruction of the external ear.

Authors:  R C TANZER
Journal:  Plast Reconstr Surg Transplant Bull       Date:  1959-01

3.  Congenital microtia and meatal atresia; observations and aspects of treatment.

Authors:  Y MEURMAN
Journal:  AMA Arch Otolaryngol       Date:  1957-10

Review 4.  Relations and interactions between cranial mesoderm and neural crest populations.

Authors:  Drew M Noden; Paul A Trainor
Journal:  J Anat       Date:  2005-11       Impact factor: 2.610

5.  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

6.  Deletion of 1q in a patient with acrofacial dysostosis.

Authors:  D J Waggoner; D J Ciske; S B Dowton; M S Watson
Journal:  Am J Med Genet       Date:  1999-02-12

7.  A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate.

Authors:  Maria Leine Guion-Almeida; Roseli Maria Zechi-Ceide; Siulan Vendramini; Alfredo Tabith Júnior
Journal:  Clin Dysmorphol       Date:  2006-07       Impact factor: 0.816

8.  Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis.

Authors:  Amy E Merrill; Elena G Bochukova; Sean M Brugger; Mamoru Ishii; Daniela T Pilz; Steven A Wall; Karen M Lyons; Andrew O M Wilkie; Robert E Maxson
Journal:  Hum Mol Genet       Date:  2006-03-15       Impact factor: 6.150

9.  Developmental expression of the murine spliceosome-associated protein mSAP49.

Authors:  P Ruiz-Lozano; P Doevendans; A Brown; P J Gruber; K R Chien
Journal:  Dev Dyn       Date:  1997-04       Impact factor: 3.780

10.  Msx2 gene dosage influences the number of proliferative osteogenic cells in growth centers of the developing murine skull: a possible mechanism for MSX2-mediated craniosynostosis in humans.

Authors:  Y H Liu; Z Tang; R K Kundu; L Wu; W Luo; D Zhu; F Sangiorgi; M L Snead; R E Maxson
Journal:  Dev Biol       Date:  1999-01-15       Impact factor: 3.582

View more
  33 in total

1.  The Mighty Chondrocyte: No Bones about It.

Authors:  P Purcell; P A Trainor
Journal:  J Dent Res       Date:  2015-09-04       Impact factor: 6.116

2.  Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome.

Authors:  Catherine Bélanger; Félix-Antoine Bérubé-Simard; Elizabeth Leduc; Guillaume Bernas; Philippe M Campeau; Seema R Lalani; Donna M Martin; Stephanie Bielas; Amanda Moccia; Anshika Srivastava; David W Silversides; Nicolas Pilon
Journal:  Proc Natl Acad Sci U S A       Date:  2018-01-08       Impact factor: 11.205

Review 3.  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 4.  Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology.

Authors:  Peter G Farlie; Naomi L Baker; Patrick Yap; Tiong Y Tan
Journal:  Mol Syndromol       Date:  2016-10-29

5.  Facing up to the challenges of advancing Craniofacial Research.

Authors:  Paul A Trainor; Joan T Richtsmeier
Journal:  Am J Med Genet A       Date:  2015-03-28       Impact factor: 2.802

6.  Fetal Skeletal Dysplasias that Involve the Face: Binder Syndrome and Nager Syndrome.

Authors:  Alina Veduta; Simona Duta; Anca Marina Ciobanu; Radu Botezatu; Nicolae Gica; Gheorghe Peltecu; Anca Maria Panaitescu
Journal:  Maedica (Bucur)       Date:  2021-03

7.  Treacher Collins syndrome mutations in Saccharomyces cerevisiae destabilize RNA polymerase I and III complex integrity.

Authors:  Nancy Walker-Kopp; Ashleigh J Jackobel; Gianno N Pannafino; Paola A Morocho; Xia Xu; Bruce A Knutson
Journal:  Hum Mol Genet       Date:  2017-11-01       Impact factor: 6.150

8.  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

9.  Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome.

Authors:  Arun Devotta; Hugo Juraver-Geslin; Jose Antonio Gonzalez; Chang-Soo Hong; Jean-Pierre Saint-Jeannet
Journal:  Dev Biol       Date:  2016-02-11       Impact factor: 3.582

10.  Acrofacial Dysostosis, Cincinnati Type, a Mandibulofacial Dysostosis Syndrome with Limb Anomalies, Is Caused by POLR1A Dysfunction.

Authors:  K Nicole Weaver; Kristin E Noack Watt; Robert B Hufnagel; Joaquin Navajas Acedo; Luke L Linscott; Kristen L Sund; Patricia L Bender; Rainer König; Charles M Lourenco; Ute Hehr; Robert J Hopkin; Dietmar R Lohmann; Paul A Trainor; Dagmar Wieczorek; Howard M Saal
Journal:  Am J Hum Genet       Date:  2015-04-23       Impact factor: 11.025

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.