Goldenhar Syndrome Associated with Bilateral Ocular Choristomas and Cardiac Abnormalities*
نویسندگان
چکیده
*This report presented in 36th National Congress of Turk Ophthalmology Society in October 2002, Ankara, Turkey. This study presents a report on a 14-year-old male with Goldenhar syndrome featuring bilateral epibulbar mass, right hemifacial microsomia, deafness, and right scoliozis. Cardiac disorders including systolic murmur, sinusoidal arrhythmia, and prolapse of mitral valve were detected in the case. Goldenhar syndrome needs to a multidisciplinary approach regarding craniofacial and cardiologic associations. Ophthalmologists should focus on visual sequels and amblyopia.
منابع مشابه
سندرم گلدنهار
Background : Hemifacial microsomia or Goldenhar syndrome is a congenital abnormality that it's main features are an one-sided under development of ear (or Artesia), jaw and neck. This syndrome is associated with additional anomalies and from view point of phenotype is highly variable. Case Report: The case was a one day old girl born to a 30 years old woman by normal vaginal delivery. Conge...
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