Literature DB >> 19736507

Craniofacial features in Goldenhar syndrome.

C Vinay1, R Sudhakara Reddy, K S Uloopi, V Madhuri, R Chandra Sekhar.   

Abstract

Goldenhar syndrome also known as oculo-auriculo-vertebral syndrome was first reported by Dr Maurice Goldenhar in 1952. It is a rare disease entity characterized by craniofacial anomalies such as hypoplasia of the mandible and malar bones, microtia, and vertebral anomalies. The etiology of this disease still remains unclear and occurs as sporadic. This report presents goldenhar syndrome in a 12-year-old male patient.

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Year:  2009        PMID: 19736507     DOI: 10.4103/0970-4388.55339

Source DB:  PubMed          Journal:  J Indian Soc Pedod Prev Dent        ISSN: 0970-4388


  6 in total

1.  Role of 3D-CT for orthodontic and ENT evaluation in Goldenhar syndrome.

Authors:  S Saccomanno; F Greco; L D'Alatri; E De Corso; M Pandolfini; B Sergi; T Pirronti; R Deli
Journal:  Acta Otorhinolaryngol Ital       Date:  2014-08       Impact factor: 2.124

2.  Lipodermoid Cyst: A Report of a Rare Caruncular Case.

Authors:  Mohammad Taher Rajabi; Koosha Ramezani
Journal:  Middle East Afr J Ophthalmol       Date:  2015 Oct-Dec

3.  Goldenhar Syndrome: A Case Report with Review.

Authors:  Mridula Goswami; Urvashi Bhushan; Babita Jangra
Journal:  Int J Clin Pediatr Dent       Date:  2016-09-27

4.  Hemifacial Microsomia and Accessory Auricles in an Adolescent Boy.

Authors:  C Chandrakala; Parimalam Kumar; B Karpagam
Journal:  Indian J Dermatol       Date:  2017 Mar-Apr       Impact factor: 1.494

5.  Goldenhar Syndrome with Dextrocardia and Right Pulmonary Hypoplasia: An Unusual Association.

Authors:  Nagendra Chaudhary; Sandeep Shrestha; Hemant Kumar Halwai
Journal:  Case Rep Genet       Date:  2017-03-09

6.  [Diffuse brain atrophy in a Goldenhar syndrome: report of a case].

Authors:  Yogolelo Asani; Cilundika Mulenga; Léon Kabamba Ngombe; Kalenga Muenze; Chenge Borasisi
Journal:  Pan Afr Med J       Date:  2014-10-13
  6 in total

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