Goldenhar Syndrome–A   Case Report

Vidya HOLLA; Raghavendra KİNİ; Prassana KUMAR RAO; Roopashri KASHYAP; Devika SHETTY; Kamakshi JHA

doi:https://doi.org/10.7126/cumudj.454491

Makale detayları

Goldenhar Syndrome–A Case Report

Yazarlar:

Vidya HOLLA | Raghavendra KİNİ | Prassana KUMAR RAO | Roopashri KASHYAP | Devika SHETTY | Kamakshi JHA

Ana Başlıklar:

Sağlık teşvikleri

Dergi:

Cumhuriyet Dental Journal 2019 Vol.22 Issue 1, pp.131-135

Belge Tipi:

Makale

Yayın Tarihi:

3/2019

Belge Dili:

İngilizce

Document ID (Org No.):

2000734674

DOI:

https://doi.org/10.7126/cumudj.454491

Özet:

 

Goldenhar Syndrome also called as facio-auriculo-vertebral
dysplasia, is a rare syndrome developing from first and second
pharyngeal arches during Blastogenesis. It was described by Maurice Goldenhar in
1952. It is characterised by presence of epibulbar dermoids, ear malformations,
vertebral anomalies, unilateral facial hypoplasia, and sometimes internal
systemic complications. As the molecular basis for Goldenhar Syndrome is unclear,
early detection and screening for complications would help the patients to have
a normal life.

Makale detayları

Goldenhar Syndrome–A Case Report

Yazarlar: Vidya HOLLA | Raghavendra KİNİ | Prassana KUMAR RAO | Roopashri KASHYAP | Devika SHETTY | Kamakshi JHA

Ana Başlıklar: Sağlık teşvikleri

Dergi: Cumhuriyet Dental Journal 2019 Vol.22 Issue 1, pp.131-135

Belge Tipi: Makale

Yayın Tarihi: 3/2019

Belge Dili: İngilizce

Document ID (Org No.): 2000734674

DOI: https://doi.org/10.7126/cumudj.454491

Sayı

Yazarlar:

Vidya HOLLA | Raghavendra KİNİ | Prassana KUMAR RAO | Roopashri KASHYAP | Devika SHETTY | Kamakshi JHA

Ana Başlıklar:

Sağlık teşvikleri

Dergi:

Cumhuriyet Dental Journal 2019 Vol.22 Issue 1, pp.131-135

Belge Tipi:

Makale

Yayın Tarihi:

3/2019

Belge Dili:

İngilizce

Document ID (Org No.):

2000734674

DOI:

https://doi.org/10.7126/cumudj.454491