1.
Journal of the Korean Society of Neonatology
;
: 59-63, 2000.
Article
in Korean
| WPRIM
| ID: wpr-202535
ABSTRACT
Schinzel-Giedion syndrome is a rare autosomal recessive condition characterized by a typical face including midface retraction, urogenital anomalies, and skeletal manifestations. So far 30 patients have been reported. This is the first report of this syndrome demonstrated in Korea. We describe a male infant with the typical findings of Schinzel-Giedion syndrome, also showing sacrococcygeal teratoma.