Ahmet KÖSE, Mehmet ELTAN, Ali Evren BİLGİÇ, Yusuf KALE

Adams-Oliver Sendromlu Bir Prematüre Yeni Doğan: Olgu Sunumu ve Literatür Değerlendirmesi

Adams-Oliver sendromu, ilk kez 1945 yılında tanımlanmıştır. Kutis aplazisi ve sıklıkla saçlı deri altındaki kemik dokuda defekt ve distal ekstremite anomalileriyle karakterize nadir herediter bir hastalıktır. Fizik muayene ve radyolojik bulgular ile Adams-Oliver sendromu tanısı düşünülmüş olan bu vaka nadir görülmesi nedeniyle literatür bilgileri ile birlikte sunulmuştur.

A Preterm Newborn with Adams Oliver Syndrome: A Case Report and Review of the Literature

A Preterm Newborn with Adams Oliver Syndrome: A Case Report and Review of the Literature Adams Oliver syndrome was first described in 1945. It is a hereditary disease characterised by aplasia cutis congenita, bone defect underlying the scalp and terminal transverse limb defects of variable severity. This case, diagnosed as Adams-Oliver syndrome by physical examination and radiological findings, is presented because of its rarity, with a review of the literature.

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