Introduction: The oculo-auriculo-vertebral syndrome is a complex disease of the head and neck. Aim: The purpose of this study was to look for facial asymmetry, measuring both sides of the mandible and external ear in ...Introduction: The oculo-auriculo-vertebral syndrome is a complex disease of the head and neck. Aim: The purpose of this study was to look for facial asymmetry, measuring both sides of the mandible and external ear in the parents of these patients in a clinical way, to see if it could be considered as a minor manifestation of the disease. Patients and Methods: A clinical, observational study was done with 50 trios and their parents’ controls, at the Instituto Nacional de Rehabilitación LGII in 2019, from January to May. Mandible and ear measurements were done. Results: All of our patients had microtia and facial asymmetry, and in 17 cases, other anomalies. We compared both sides of the mandible in the patients’ parents and in the parents’ controls. The results showed differences only in the fathers, and in the comparison with the controls, we found statistical differences only in women, family and non-family cases. The ears did not show any differences. Discussion: It is very interesting that we found differences in the measurements of the mandible of the patients’ mothers and their controls;in the mothers the mandible was bigger than in the controls, this probably means that the development of the cranial structures is modified by some genetic variants. No differences were found in the measurements of the ears. Conclusion: It is very difficult to know exactly if the differences we found are important or not. The clinical measurements could be a good option to establish if the parents have minor manifestations that could explain some heritability.展开更多
Goldenhar syndrome(oculo-auriculo-vertebral spectrum)is a rare congenital anomaly of unclear etiology and characterized by craniofacial anomalies such as hemifacial microsomia,auricular,ocular and vertebral anomalies....Goldenhar syndrome(oculo-auriculo-vertebral spectrum)is a rare congenital anomaly of unclear etiology and characterized by craniofacial anomalies such as hemifacial microsomia,auricular,ocular and vertebral anomalies.In many cases,this syndrome goes unnoticed due to a lack of knowledge about its features and because of its associated wide range of overlapping anomalies.Herewith,we present a case of Goldenhar syndrome in a 21-year-old male,who presented all the classical signs of this rare condition.This article also summarizes the characteristic features of patients with Goldenhar syndrome.展开更多
文摘Introduction: The oculo-auriculo-vertebral syndrome is a complex disease of the head and neck. Aim: The purpose of this study was to look for facial asymmetry, measuring both sides of the mandible and external ear in the parents of these patients in a clinical way, to see if it could be considered as a minor manifestation of the disease. Patients and Methods: A clinical, observational study was done with 50 trios and their parents’ controls, at the Instituto Nacional de Rehabilitación LGII in 2019, from January to May. Mandible and ear measurements were done. Results: All of our patients had microtia and facial asymmetry, and in 17 cases, other anomalies. We compared both sides of the mandible in the patients’ parents and in the parents’ controls. The results showed differences only in the fathers, and in the comparison with the controls, we found statistical differences only in women, family and non-family cases. The ears did not show any differences. Discussion: It is very interesting that we found differences in the measurements of the mandible of the patients’ mothers and their controls;in the mothers the mandible was bigger than in the controls, this probably means that the development of the cranial structures is modified by some genetic variants. No differences were found in the measurements of the ears. Conclusion: It is very difficult to know exactly if the differences we found are important or not. The clinical measurements could be a good option to establish if the parents have minor manifestations that could explain some heritability.
文摘Goldenhar syndrome(oculo-auriculo-vertebral spectrum)is a rare congenital anomaly of unclear etiology and characterized by craniofacial anomalies such as hemifacial microsomia,auricular,ocular and vertebral anomalies.In many cases,this syndrome goes unnoticed due to a lack of knowledge about its features and because of its associated wide range of overlapping anomalies.Herewith,we present a case of Goldenhar syndrome in a 21-year-old male,who presented all the classical signs of this rare condition.This article also summarizes the characteristic features of patients with Goldenhar syndrome.
