Literature DB >> 25118188

Oculo-auriculo-vertebral spectrum: a review of the literature and genetic update.

Ana Beleza-Meireles1, Jill Clayton-Smith2, Jorge M Saraiva3, May Tassabehji2.   

Abstract

Oculo-auriculo-vertebral spectrum (OAVS, OMIM 164 210) is a developmental disorder primarily involving structures derived from the first and second pharyngeal arches during embryogenesis. The phenotype is clinically heterogeneous and is typically characterised by abnormal development of the ear, mandible anomalies and defects of the vertebral column. OAVS may occur as a multiple congenital abnormality, and associated findings include anomalies of the eye, brain, heart, kidneys and other organs and systems. Both genetic and environmental factors are thought to contribute to this craniofacial condition, however, the mechanisms are still poorly understood. Here, we present a review of the literature on OAVS, discussing what is known about the aetiology, candidate loci, possible mechanisms and the range of clinical features that characterise this condition. We also comment on some important aspects of recurrence risk counselling to aid clinical management. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Clinical genetics; Developmental; Genetics; Microarray; Molecular genetics

Mesh:

Year:  2014        PMID: 25118188     DOI: 10.1136/jmedgenet-2014-102476

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


  26 in total

1.  A novel de novo mutation in MYT1, the unique OAVS gene identified so far.

Authors:  Marie Berenguer; Angele Tingaud-Sequeira; Mileny Colovati; Maria I Melaragno; Silvia Bragagnolo; Ana B A Perez; Benoit Arveiler; Didier Lacombe; Caroline Rooryck
Journal:  Eur J Hum Genet       Date:  2017-06-14       Impact factor: 4.246

2.  Methods and Challenges in a Cohort Study of Infants and Toddlers With Craniofacial Microsomia: The Clock Study.

Authors:  Daniela V Luquetti; Matthew L Speltz; Erin R Wallace; Babette Siebold; Brent R Collett; Amelia F Drake; Alexis L Johns; Kathleen A Kapp-Simon; Sara L Kinter; Brian G Leroux; Leanne Magee; Susan Norton; Kathleen Sie; Carrie L Heike
Journal:  Cleft Palate Craniofac J       Date:  2019-01-08

3.  Goldenhar Syndrome with Imperforate Anus: New Association or Coincidence!

Authors:  Indar Kumar Sharawat; Deepanjan Bhattacharya; Lokesh Saini
Journal:  Indian J Pediatr       Date:  2019-07-13       Impact factor: 1.967

4.  Evaluation of prenatal diabetes mellitus and other risk factors for craniofacial microsomia.

Authors:  Babette Siebold; Carrie L Heike; Brian G Leroux; Matthew L Speltz; Amelia F Drake; Alexis L Johns; Kathleen A Kapp-Simon; Leanne Magee; Daniela V Luquetti
Journal:  Birth Defects Res       Date:  2019-03-30       Impact factor: 2.344

Review 5.  Goldenhar syndrome: current perspectives.

Authors:  Katarzyna Bogusiak; Aleksandra Puch; Piotr Arkuszewski
Journal:  World J Pediatr       Date:  2017-06-15       Impact factor: 2.764

Review 6.  Genetic Advances in the Understanding of Microtia.

Authors:  Craig Gendron; Ann Schwentker; John A van Aalst
Journal:  J Pediatr Genet       Date:  2016-09-23

7.  Healthcare and psychosocial experiences of individuals with craniofacial microsomia: Patient and caregivers perspectives.

Authors:  Daniela V Luquetti; Michelle R Brajcich; Nicola M Stock; Carrie L Heike; Alexis L Johns
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2018-02-07       Impact factor: 1.675

Review 8.  Hemifacial microsomia: skeletal abnormalities evaluation using CBCT (case report).

Authors:  Sergey Lvovich Kabak; Nina Alexandrovna Savrasova; Valentina Vladimirovna Zatochnaya; Yuliya Michailovna Melnichenko
Journal:  J Radiol Case Rep       Date:  2019-11-30

9.  A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR Congo.

Authors:  Aimé Lumaka; Valerie Race; Hilde Peeters; Anniek Corveleyn; Zeynep Coban-Akdemir; Shalini N Jhangiani; Xiaofei Song; Gerrye Mubungu; Jennifer Posey; James R Lupski; Joris R Vermeesch; Prosper Lukusa; Koenraad Devriendt
Journal:  Am J Med Genet A       Date:  2018-08-08       Impact factor: 2.802

10.  In Their Own Words: Caregiver and Patient Perspectives on Stressors, Resources, and Recommendations in Craniofacial Microsomia Care.

Authors:  Alexis L Johns; Daniela V Luquetti; Michelle R Brajcich; Carrie L Heike; Nicola M Stock
Journal:  J Craniofac Surg       Date:  2018-11       Impact factor: 1.046

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.