Important It is possible that the main title of the report Goldenhar Syndrome (Oculo Auriculo Vertebral Spectrum) is not the name you expected. Please ...
Goldenhar Syndrome is a congenital disease, meaning that it is present in infants when they are born. The cause is an abnormality in a chromosome, and because the ...
Goldenhar syndrome occurs sporadically in most cases. ... Read more about Manifestations of Craniofacial Syndromes on Medscape Related Reference Topics.
Goldenhar syndrome (also known as Oculo-Auriculo-Vertebral (OAV) syndrome) is a rare congenital defect characterized by incomplete development of the ear, nose, soft ...
A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Goldenhar disease
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Goldenhar syndrome is a syndrome of complex structures developing from first and second branchial arches during blastogenesis. The etiology of this rare disease is ...
Goldenhar Syndrome . Download PDF information sheet. Back to Craniofacial Anomalies. What is Goldenhar Syndrome? Goldenhar Syndrome is a congenital birth defect which ...
Goldenhar Syndrome is a congenital anomaly, meaning it is present at birth. Patients with Goldenhar Syndrome exhibit unilateral or bilateral Hemifacial Microsomia (HFM)
Goldenhar syndrome is a condition that typically causes congenital (at birth) physical abnormalities in the face or spinal column. Goldenhar syndrome is caused by a ...