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A Case of Hallermann-Streiff Syndrome with Intra-Uterine Growth Retardation

Published online September 15, 2003.
A Case of Hallermann-Streiff Syndrome with Intra-Uterine Growth Retardation
Seung Yeoun Kim, Young Min Kim, Hye Sun Yoon
Department of Pediatrics, School of Medicine, Eulji University, Seoul, Korea
자궁내 발육지연을 동반한 Hallermann Streiff 증후군 1례
김승연, 김영민, 윤혜선
을지의과대학 소아과학교실
Correspondence: 
Hye Sun Yoon, Email: yhs3211@eulji.or.kr
Abstract
Hallermann-Streiff syndrome is a rare disease; approximately 150 cases have been reported in the world literature. The syndrome consists of proportionate nanism; hypotrichosis; atrophy and extreme thinness of skin, particulary over the facial area; an usual "bird-like" face with mandibular hypoplasia; a prominent thin, pointed nose; congenital cataracts; and severe dental abnormalities. We report a case of Hallermann-Streiff syndrome in premature who showed intrauterine growth retardation with proportionate nanism, brachycephaly, a beaked nose, "bird like" face, hypoplasia of the mandible, microphthalmia, congenital cataract, neonatal teeth, and widening of sagittal suture were all found on our patient.
Key Words: brachycephaly


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