Congenital absence of the internal carotid artery (ICA) is an extremely rare vascular anomaly. Aplasia and displacement of the horizontal portion of the petrous carotid artery have been described in a patient with mandibulofacial dysostosis. To the best of our knowledge, the association between Goldenhar syndrome and ipsilateral ICA agenesis has emerged only in one case documented in the medical literature to date. We describe here a case that illustrates the association of Goldenhar syndrome with contralateral agenesis of the ICA incidentally detected on brain magnetic resonance imaging and subsequently confirmed on magnetic resonance angiography and high resolution computed tomography
Goldenhar syndrome (GS), a rare condition, occurring due to defect in development of first and secon...
Goldenhar’s syndrome is a rare condition described initially in the early 1950’s. It is characterize...
Wassim Farhat, Rechdi Ahdab, Hassan HosseiniService de Neurologie, Hôpital Henri Mondor, APHP,...
The association between Goldenhar syndrome and homolateral internal carotid artery agenesis to our k...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Goldenhar syndrome (Oculo-Auriculo-Vertebral Spectrum) (OAVS) is a rare congenital condition charact...
The internal carotid artery agenesis is a rare malformation disorder. We report the case of a 12-yea...
Goldenhar syndrome (GS) is also known as hemifacial microsomia or oculo-auriculo-vertebral dysplasia...
Goldenhar's syndrome is a rare condition described initially in the early 1950's. It is characterize...
Goldenhar syndrome (GS) is a condition with a multitude of abnormalities, classically involving ocul...
internal carotid artery (ICA) and an aortic arch anomaly that presented with ipsilateral congenital ...
Congenital unilateral agenesis of the internal carotid artery (ICA) is a rare anomaly. Due to proper...
Goldenhar syndrome (oculo-auriculo-vertebral spectrum) is a rare congenital anomaly of unclear etiol...
AbstractGoldenhar syndrome is a congenital condition that is associated with abnormalities of the he...
ABSTRACT Goldenhar Syndrome is a rare, generally sporadic condition, whose physical manifestations i...
Goldenhar syndrome (GS), a rare condition, occurring due to defect in development of first and secon...
Goldenhar’s syndrome is a rare condition described initially in the early 1950’s. It is characterize...
Wassim Farhat, Rechdi Ahdab, Hassan HosseiniService de Neurologie, Hôpital Henri Mondor, APHP,...
The association between Goldenhar syndrome and homolateral internal carotid artery agenesis to our k...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Goldenhar syndrome (Oculo-Auriculo-Vertebral Spectrum) (OAVS) is a rare congenital condition charact...
The internal carotid artery agenesis is a rare malformation disorder. We report the case of a 12-yea...
Goldenhar syndrome (GS) is also known as hemifacial microsomia or oculo-auriculo-vertebral dysplasia...
Goldenhar's syndrome is a rare condition described initially in the early 1950's. It is characterize...
Goldenhar syndrome (GS) is a condition with a multitude of abnormalities, classically involving ocul...
internal carotid artery (ICA) and an aortic arch anomaly that presented with ipsilateral congenital ...
Congenital unilateral agenesis of the internal carotid artery (ICA) is a rare anomaly. Due to proper...
Goldenhar syndrome (oculo-auriculo-vertebral spectrum) is a rare congenital anomaly of unclear etiol...
AbstractGoldenhar syndrome is a congenital condition that is associated with abnormalities of the he...
ABSTRACT Goldenhar Syndrome is a rare, generally sporadic condition, whose physical manifestations i...
Goldenhar syndrome (GS), a rare condition, occurring due to defect in development of first and secon...
Goldenhar’s syndrome is a rare condition described initially in the early 1950’s. It is characterize...
Wassim Farhat, Rechdi Ahdab, Hassan HosseiniService de Neurologie, Hôpital Henri Mondor, APHP,...