Abstract
Fraser syndrome is a rare autosomal recessive malformation syndrome characterized by cryptophthalmos, syndactyly, and laryngeal and urogenital defects. The diagnosis of this syndrome can be made on clinical examination and occasionally on prenatal ultrasound. We report a newborn who presented with respiratory failure in the neonatal intensive care unit and was diagnosed as Fraser syndrome with clinical findings such as cryptophthalmos, syndactyly, anal atresia, and laryngeal atresia.
Keywords: Fraser sendromu, kriptooftalmus, sindaktili, larengeal stenoz.
How to Cite
1.
Kavurt S, Özcan B, Baş ÖAAY, Demirel N. Fraser syndrome: a case report. Çocuk Sağlığı ve Hastalıkları Dergisi 2013; 56: 20-3. Available from: https://cshd.org.tr/article/view/166