AbstractGoldenhar syndrome is a congenital condition that is associated with abnormalities of the head and the bones of the spinal column. The abnormalities of the head can include anomalies of the eyes, ears, facial bones, and mouth. These anomalies are extremely variable in severity. The exact cause of Goldenhar syndrome remains unknown. The etiology of this rare disease is not fully understood, as it has shown itself variable genetically and of unclear causes. This work reports a case of Goldenhar syndrome in a 1-year-old female, who presented some of the classical signs of this rare condition including Hemifacial Microsomia, epibulber dermoid tumor and preauricular skin tags. However, vertebral anomalies, deafness, renal and cardiac ano...
Goldenhar syndrome (GS) is a condition with a multitude of abnormalities, classically involving ocul...
Goldenhar's syndrome - also known as facio-auricolo-vertebral spectrum - is due to a developmental d...
Relative importance of the current issue is based on rare occurrence of this dermatosis, its genetic...
AbstractGoldenhar syndrome is a congenital condition that is associated with abnormalities of the he...
Goldenhar syndrome is a congenital condition that is associated with abnormalities of the head and t...
Goldenhar's syndrome is a rare condition described initially in the early 1950's. It is characterize...
Goldenhar’s syndrome is a rare condition described initially in the early 1950’s. It is characterize...
Goldenhar syndrome (GS) is also known as hemifacial microsomia or oculo-auriculo-vertebral dysplasia...
ABSTRACT Goldenhar Syndrome is a rare, generally sporadic condition, whose physical manifestations i...
Goldenhar syndrome (oculo-auriculo-vertebral spectrum) is a rare congenital anomaly of unclear etiol...
Goldenhar syndrome is a sporadic or inherited genetic syndrome characterized by limbal dermoids, pre...
Goldenhar syndrome (Oculo-Auriculo-Vertebral Spectrum) (OAVS) is a rare congenital condition charact...
Goldenhar Syndrome also called as facio-auriculo-vertebral dysplasia, is a rare syndrome developing ...
Goldenhar syndrome is a rare congenital anomaly which consists of a triad of an ocular dermoid cyst,...
Goldenhar syndrome (GS), a rare condition, occurring due to defect in development of first and secon...
Goldenhar syndrome (GS) is a condition with a multitude of abnormalities, classically involving ocul...
Goldenhar's syndrome - also known as facio-auricolo-vertebral spectrum - is due to a developmental d...
Relative importance of the current issue is based on rare occurrence of this dermatosis, its genetic...
AbstractGoldenhar syndrome is a congenital condition that is associated with abnormalities of the he...
Goldenhar syndrome is a congenital condition that is associated with abnormalities of the head and t...
Goldenhar's syndrome is a rare condition described initially in the early 1950's. It is characterize...
Goldenhar’s syndrome is a rare condition described initially in the early 1950’s. It is characterize...
Goldenhar syndrome (GS) is also known as hemifacial microsomia or oculo-auriculo-vertebral dysplasia...
ABSTRACT Goldenhar Syndrome is a rare, generally sporadic condition, whose physical manifestations i...
Goldenhar syndrome (oculo-auriculo-vertebral spectrum) is a rare congenital anomaly of unclear etiol...
Goldenhar syndrome is a sporadic or inherited genetic syndrome characterized by limbal dermoids, pre...
Goldenhar syndrome (Oculo-Auriculo-Vertebral Spectrum) (OAVS) is a rare congenital condition charact...
Goldenhar Syndrome also called as facio-auriculo-vertebral dysplasia, is a rare syndrome developing ...
Goldenhar syndrome is a rare congenital anomaly which consists of a triad of an ocular dermoid cyst,...
Goldenhar syndrome (GS), a rare condition, occurring due to defect in development of first and secon...
Goldenhar syndrome (GS) is a condition with a multitude of abnormalities, classically involving ocul...
Goldenhar's syndrome - also known as facio-auricolo-vertebral spectrum - is due to a developmental d...
Relative importance of the current issue is based on rare occurrence of this dermatosis, its genetic...