PİERRE ROBİN SENDROMLU BİR HASTADA HIZLI ÜST ÇENE GENİŞLETMESİ İLE MAKSİLLER DARLIK VE MANDİBULADAKİ KAYMANIN DÜZELTİLMESİ: OLGU SUNUMU

Abstract

Pierre Robin sendromunda konjenital kalp defektleri, iskeletsel anomaliler, göz ve kulak sorunları gibi sistemik bulgular ve ayrıca mikrognati, yarık damak gibi çene yüz bölgesi anomalileri görülebilmektedir. Ek olarak, bu hastaların birçoğunda dişsel problemler bulunmaktadır. Neonatal dönemde yeterli solunum ve beslenmenin sağlanabildiği olgularda normal büyüme gelişme elde edilebilir. Fakat maksilladaki yarık sahası ile mandibuladaki mikrognati varlığı daimi dişlenmeyle beraber dişsel problemleri beraberinde getirir. Bu olgu sunumunda, doğumda tanımlanmış ve sonraki yıllarda yarık damağın tedavi edilmiş olduğu ve ortodontik tedavisi halen devam etmekte olan bir Pierre Robin olgusu sunulmuştur

Correction of transversal maxillary discrepancy and Mandibular sliding with Rapid Maxillar Expansion of a Pierre Robin Syndrome Patient: Case Report

Abstract

In Pierre Robin syndrome, systemic findings such as congenital heart defects, skeletal anomalies, eye and ear problems, as well as chin facial anomalies such as micrognathia and cleft palate can be seen. In addition, most of these patients have dental problems. In cases, where adequate respiration and feeding are provided during neonatal period, normal growth can be achieved. However, the maxil lary cleft area and the presence of the micrognathia in the mandible bring dental problems together with permanent teeth. In this study, a case report of Pierre Robin syndrome is presented who was diagnosed at birth and associated cleft palate has been treated through the intervening years and at present her orthodontic treatment is continuing.

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