Goldenhar Syndrome. Case report
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Keywords
malformation
microtia
branchial arch
Abstract
Goldenhar syndrome is the second most common craniofacial malformation; it ca be sporadic presentation or as autosomal-dominant inheritance, it involves the organs derived from the first and second branchial arches. Its main characteristics are ocular, auricular (ear and pinna) and vertebral affections. We present the case of a newborn product of a 40-year-old mother with a history of Gestational Diabetes and Uterine Fibromatosis, with preterm labor.
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References
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Wang R, Martínez-Frías ML, Graham JM Jr. Infants of diabetic mothers are at increased risk for the oculo-auriculo-vertebral sequence: a case-based and case-control approach. J Pediatr. 2002;141:611-7.