All issues > Volume 46(9); 2003

Erratum

J Korean Pediatr Soc. 2003;46:0. Published online September 15, 2003.

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

Seung Yeoun SY Kim¹, Young Min YM Kim¹, Hye Sun HS Yoon¹

¹Department of Pediatrics, School of Medicine, Eulji University, Seoul, Korea

Correspondence Hye Sun HS 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.

Keywords :brachycephaly