Hallermann-Streiff Syndrome: Case report

Hallermann-Streiff Syndrome is a considerably rare disorder that is principally diagnosed by multiple congenital anomalies observed in the head and neck region. It was first identified in 1948 by Hallermann and then in 1950 by Streiff. The most frequently encountered clinical characteristics of the syndrome are bird-like facial appearance, hypoplastic mandible and maxilla, eye and teeth anomalies, skin atrophy, particularly on the nose, and short stature. Because of the rarity of this syndrome, this paper presents a neonate with Hallermann-Streiff Syndrome together with a description of the newborn’s clinical characteristics.

Hallermann-Streiff Sendromu: Olgu sunumu

Hallermann-Streiff Sendromu oldukça nadir görülen ve esas olarak baþ-boyun bölgesindeki multipl konjenital anomaliler ile taný alan bir sendromdur. ilk kez 1948 yýlýnda Hallermann daha sonra 1950 yýlýnda Streiff tarafýndan tanýmlanmýþtýr. En sýk gözlenen klinik özellikler kuþa benzer yüz görünümü, mandibula ve maksilla hipoplazisi, göz ve diþ anomalileri, özellikle burun üzerindeki cilt atrofisi ve ufak vücut yapýsýdýr. Bu yazýda oldukça nadir görülmesi nedeniyle Hallermann-Streiff Sendromlu bir yenidoðan ve klinik özellikleri sunulmuþtur.