CROUZON SYNDROME - CLINICAL-EVOLUTIVE PARTICULARITIES. CASE REPORT

• Asıl Yazarlar: Aniko Maria Manea (Yazar), Nicoleta Kiritescu (Yazar), Dobre Mihaela (Yazar), Mariana Boia (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Amaltea Medical Publishing House, 2016-03-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

The Crouzon's Syndrome is a rare genetic disorder, with an incidence between 1/25,000 to 1/100,000 newborn babies, transmitted autosomal dominant, characterized by facial dysmorphism and craniosynostosis, based on those characteristic can be diagnosed early. We present the case of a premature n...