AI Summary & Key Takeaways
AI InsightIn this article, we present a 2- month-old case with recurrent urinary tract infections, skeletal and ear anomalies accompanied by Goldenhar syndrome.
📌 3 Key Takeaways
Abstract
Goldenhar syndrome is a rare disease characterized by anomalies of the ear, eye and vertebrae, caused by developmental failure of the first and second brachial arches. Genitourinary, cardiac, skeletal and central nervous system anomalies can also be seen in addition to craniofacial anomalies. In this article, we present a 2- month-old case with recurrent urinary tract infections, skeletal and ear anomalies accompanied by Goldenhar syndrome.
Özet
Goldenhar sendromu göz, kulak ve vertebra anomalileri ile karakterize, birinci ve ikinci brakiyal arkın gelişim anomalisine bağlı olarak görülen bir hastalıktır. Kraniofasiyal anomalilere genitoüriner, kardiyak, iskelet ve santral sinir sistemi anomalileri de eşlik edebilir. Bu yazıda tekrarlayan idrar yolu enfeksiyonu olan, iskelet ve kulak anomalilerinin eşlik ettiği ve Goldenhar sendromu tanısı koyulan 2 aylık olgu sunulmuştur.