Literature DB >> 16186139

Goldenhar's syndrome associated with multiple congenital abnormalities.

Suleyman Bayraktar1, Seher Tabanli Bayraktar, Emel Ataoglu, Ayse Ayaz, Murat Elevli.   

Abstract

Goldenhar's syndrome is characterized by a combination of dermal epibulbar cysts, auricular appendices, malformation of ears, and vertebral anomalies. The average incidence ratio of Goldenhar's syndrome is estimated to be 1/5600, and the frequency of cardiovascular malformations of this syndrome is 5-58 per cent. Although the etiology of this disease is not fully understood, autosomal recessive or dominant inheritance is possible. The disease occurs as sporadic cases. Male:female ratio for the Goldenhar's syndrome is 2:1. A 72-day-old Goldenhar's syndrome case is reported who presented with multiple congenital anomalies.

Entities:  

Mesh:

Year:  2005        PMID: 16186139     DOI: 10.1093/tropej/fmi020

Source DB:  PubMed          Journal:  J Trop Pediatr        ISSN: 0142-6338            Impact factor:   1.165


  3 in total

1.  Ophthalmic features and management outcomes of 30 children having Goldenhar syndrome.

Authors:  Manpreet Singh; Manpreet Kaur; Aditi Mehta Grewal; Sonam Yangzes; Deepti Yadav; Zoramthara Zadeng; Pankaj Gupta
Journal:  Int Ophthalmol       Date:  2019-11-23       Impact factor: 2.031

2.  Specific entities affecting the craniocervical region: syndromes affecting the craniocervical junction.

Authors:  Arnold H Menezes; Timothy W Vogel
Journal:  Childs Nerv Syst       Date:  2008-03-28       Impact factor: 1.475

3.  Craniofacial Microsomia: Goldenhar Syndrome in Association with Bilateral Congenital Cataract.

Authors:  U D Shrestha; S Adhikari
Journal:  Case Rep Ophthalmol Med       Date:  2015-10-08
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.