[ Le syndrome de Goldenhar: A propos d’un cas ]
Volume 30, Issue 1, July 2020, Pages 121–124
Mariam Erradi1, Soukaina Sediki2, Ilham Tadmouri3, and Moustapha Hida4
1 Faculté de Médecine et de Pharmacie de Fès, Université Sidi Mohamed Ben Abdellah, Fès, Morocco
2 Faculté de Médecine et de Pharmacie de Fès, Université Sidi Mohamed Ben Abdellah, Fès, Morocco
3 Faculté de Médecine et de Pharmacie de Fès, Université Sidi Mohamed Ben Abdellah, Fès, Morocco
4 Service de pédiatrie et des urgences pédiatriques, Hôpital Mère - Enfant, CHU Hassan II, Fès, Morocco
Original language: French
Copyright © 2020 ISSR Journals. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Goldenhar syndrome is a rare congenital disease, affecting many organs including the craniofacial region. Its etiology still remains uncertain. We describe a case of Goldenhar syndrome in a 12-month-old infant with craniofacial involvement.This anatomical-clinical entity gives rise to a good clinical examination and a good analysis of the literature in order to make the diagnosis and to plan a treatment in the event of systemic involvement.
Author Keywords: goldenhar syndrome, mandibular hypoplasia, periauricular tags.
Volume 30, Issue 1, July 2020, Pages 121–124
Mariam Erradi1, Soukaina Sediki2, Ilham Tadmouri3, and Moustapha Hida4
1 Faculté de Médecine et de Pharmacie de Fès, Université Sidi Mohamed Ben Abdellah, Fès, Morocco
2 Faculté de Médecine et de Pharmacie de Fès, Université Sidi Mohamed Ben Abdellah, Fès, Morocco
3 Faculté de Médecine et de Pharmacie de Fès, Université Sidi Mohamed Ben Abdellah, Fès, Morocco
4 Service de pédiatrie et des urgences pédiatriques, Hôpital Mère - Enfant, CHU Hassan II, Fès, Morocco
Original language: French
Copyright © 2020 ISSR Journals. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Goldenhar syndrome is a rare congenital disease, affecting many organs including the craniofacial region. Its etiology still remains uncertain. We describe a case of Goldenhar syndrome in a 12-month-old infant with craniofacial involvement.This anatomical-clinical entity gives rise to a good clinical examination and a good analysis of the literature in order to make the diagnosis and to plan a treatment in the event of systemic involvement.
Author Keywords: goldenhar syndrome, mandibular hypoplasia, periauricular tags.
Abstract: (french)
Le syndrome de Goldenhar est une pathologie congénitale rare, affectant plusieurs organes notamment la région craniofaciale. Son étiologie reste encore mal connue. Nous décrivons un cas de syndrome de Goldenhar chez un nourrisson de 12 mois avec une atteinte craniofaciale.Cette entité anatomo-clinique suscite un bon examen clinique et une bonne analyse de la littérature afin de poser le diagnostic rapidement et de prévoir un traitement en cas d’atteinte systémique.
Author Keywords: syndrome de Goldenhar, hypoplasie mandibulaire, tragus péri-auriculaire.
How to Cite this Article
Mariam Erradi, Soukaina Sediki, Ilham Tadmouri, and Moustapha Hida, “Goldenhar syndrome: A case report,” International Journal of Innovation and Applied Studies, vol. 30, no. 1, pp. 121–124, July 2020.
