Literature DB >> 20152949

Autosomal dominant microtia.

S Chafai Elalaoui1, I Cherkaoui Jaouad, L Rifai, A Sefiani.   

Abstract

Microtia (MIM600674) is a congenital malformation which occurs in 1/8000-10000 births. It is characterized by a small, and abnormally shaped pinna. It ranges in severity from a bump of tissue to a partially formed ear cup. Microtia is often associated with atresia of the external auditory canal. Familial microtia with meatal atresia has been reported, either with dominant or recessive inheritance, which makes genetic counselling difficult in sporadic cases. In the present paper, we report the case of a family with congenital microtia and conductive deafness in two generations, suggesting autosomal dominant inheritance with variable expression and incomplete penetrance. Copyright 2010 Elsevier Masson SAS. All rights reserved.

Entities:  

Mesh:

Year:  2010        PMID: 20152949     DOI: 10.1016/j.ejmg.2010.02.002

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  4 in total

Review 1.  Genetic Advances in the Understanding of Microtia.

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

Review 2.  Microtia: epidemiology and genetics.

Authors:  Daniela V Luquetti; Carrie L Heike; Anne V Hing; Michael L Cunningham; Timothy C Cox
Journal:  Am J Med Genet A       Date:  2011-11-21       Impact factor: 2.802

3.  Johnson-McMillin Microtia Syndrome: New Additional Family.

Authors:  Nagwa Abdel-Meguid; Ola Hosny Gebril; Ehab Ragaa Abdelraouf; Mohammed Akmal Shafie; Mohammed Bahgat
Journal:  J Family Med Prim Care       Date:  2014-07

4.  Whole-Exome Sequencing of Discordant Monozygotic Twin Families for Identification of Candidate Genes for Microtia-Atresia.

Authors:  Xinmiao Fan; Lu Ping; Hao Sun; Yushan Chen; Pu Wang; Tao Liu; Rui Jiang; Xuegong Zhang; Xiaowei Chen
Journal:  Front Genet       Date:  2020-10-22       Impact factor: 4.599

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.