- Case Report
- A Case of Synophthalmia with Chromosomal Anomaly: 46,XX,-15,t(15q,21q)
-
Byung Moon Ahn, Woo Seog Kim, Moo Yung Song, Un Jun Hyoung, Jin Oh Lee
-
Clin Exp Pediatr. 1994;37(6):854-860. Published online June 15, 1994
-
|
A synophthalmia, another form of cyclopia, in which the element of the two eyes are partially fused to form an apparently single eye in the middle of the forehead. The synophthalmia is a result of complex, neural plate misdevelopment syndrome involving the eye, brain, skull and face. It is well known that synophthalmia is due to heterogenous causes, most of... |
-
-
- A Case of Unialteral Megalencephaly
-
Woo Seok Kim, Nam Soo Park, Moo Young Song, Un Jun Hyoung, Jin Oh Lee, Yong Seung Hwang
-
Clin Exp Pediatr. 1993;36(6):877-881. Published online June 15, 1993
-
|
The unilateral megalencephaly is a rare brain malfromation characterized by cerebral asymmetry and cortical dysplasia caused by faulty migration of the subependymal neuroblasts.
We experienced a case of unilateral megalencephaly in a two day-old male with the chief complaint of asymmetric head appearance. Large left hemisphere with agyria, pachygyria. dilatation of lateral ventricle, and the thick cortex of the ipsilteral hemisphere... |
-
-
- Original Article
- Clinical Analysis of Retinopathy of Prematurity
-
Nam Su Park, Young Myoung Cho, Mu Young Song, Un Jun Hyoung, Jin Oh Lee
-
Clin Exp Pediatr. 1993;36(11):1562-1569. Published online November 15, 1993
-
|
One hundred eighty infants with oxygen therapy who were under 2,500gm birth weight or under 37 weeks of gestational age, were examined between January 1990 and November 1992. We performed clinical analysis and results were as follows.
1) Fifty six infants(31.3%) were diagnosed as retinopathy of prematurity.
2) The first examination was performed at 2.5 weeks of ife on average, and the... |
-
-
- Case Report
- One Case of Ruptured Aneurysm of Vein of Galen
-
Nam Soo Park, Moo Young Song, Un Jun Hyoung, Jin Oh Lee, Eun Ryoung Kim
-
Clin Exp Pediatr. 1992;35(5):691-695. Published online May 15, 1992
-
|
The vein of Galen malformation is rare midline intracranial arteriovenous malformation that have been diagnosed more often at necropsy than in life.
The majority of these malformations were seen in neonate, infancy and childhood, and the clinical symptoms and prognosis were depended on age of presentation. The authors report a case of ruptured Vein of Galen aneurysmal malformation. A... |
-
-
- Original Article
- Two cases of Goldenhar syndrome.
-
Moo Young Song, Min Sik Kim, Nam Soo Park, Un Jun Hyoung, Jin Oh Lee, Eun Ryoung Kim
-
Clin Exp Pediatr. 1991;34(5):730-735. Published online May 31, 1991
-
|
Goldenhar syndrome is a pattern of malformation with wide variability of expression characterized
by epibulbar dermoids, preauricular appendages and pretragal blind-ended fistulas, and vertebral
anomalies.
We have experienced two cases of Goldenhar syndrome.
In one case multiple hemivertebrae, anomalous ribs, hydrocephalus with abscence of the septum
pellucidum and mild widening of the subarachnoid space were noted.
Diagnosis was made by physical examination and radiological findings.
A brief... |
-
-
- Case Report
- A Case of Chondroma in the Mediastinum.
-
Hyun Mee Lee, Jin Oh Lee, Hack Ki Kim, Byung Churl Lee
-
Clin Exp Pediatr. 1986;29(10):1143-1146. Published online October 31, 1986
-
|
Most chondroma often occur within or on the surface of the tubular bone and soft tissue,
and are also found in many organs, but it is extremely rare in the mediastinum. Recently, we experienced a case of chondroma of the middle mediastinum, in a 13-years old girl with intermittent chest discomfort and exertional dyspnea for several months. Diagnosis was made by... |
-
-
|