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Goldenhar syndrome is a rare disease characterized by anomalies in the ear, eye and vertebra, due to the anomalies in the development of the first and second brakial arms. In addition to craniophasial anomalies, genitourinary, heart, skeletal and central nervous system anomalies can also be observed. This article presents a two-month phenomenon of repeated urinary tract infection, accompanied by bone and ear anomalies and diagnosed with Goldenhar syndrome.
Alan : Sağlık Bilimleri
Dergi Türü : Ulusal
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