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Case Report
A Case of Arthrogryposis Multiplex Congenita with Congenital Hypertropic Pyloric Stenosis
Seung Chul Yang, So Young Kim, Hyun Hi Kim, Seung Hoon Han, Jong In Byun, Won Bae Lee
Clin Exp Pediatr. 1995;38(11):1577-1582.   Published online November 15, 1995
Arthrogryposis multiplex congenita is a congenital syndrome characterized by extreme stiffness and contracture of multiple joints and associated hypoplasia or absence of development of muscle, bone, and soft tissues; and refers to a heterogeneous group of congenital disorders of unknown but probably multiple etiologies. We present a 50 days old male baby who has had mmultiple fixed contractures of joints...
Two Cases of Hemimegalencephaly
Hee Sun Yang, Bin Jo, Seung Hoon Seung, Jong In Byun, Won Bae Lee, Byung Churl Lee, Snng Hoon Cho, Il Kwon Yang
Clin Exp Pediatr. 1992;35(11):1584-1589.   Published online November 15, 1992
Hemimegalencephaly is a rare brain malformation characterized by congenital hypertrophy of one cerebral hemisphere with ipsilateral increased volume of the white matter and dilatation of the lateral ventricle. We have experienced two cases of hemimegalencephaly in neonates who were admitted because of repetitive seizure. One case was simple hemimegalencephaly and the other case was combined by corpus callosum agenesis. Diagnosis was...
Original Article
The Factors on the Development of Coronary Arterial Involvement in Kawasaki Disease
Sang Yen Kim, Jong Hyun Kim, Jong In Byun, Won Bae Lee, Byung Churl Lee, Kyung Tai Whang, Kyong Su Lee, Sung Hoon Cho
Clin Exp Pediatr. 1992;35(10):1328-1335.   Published online October 15, 1992
In Kawasaki disease, coronary arterial involvement is an important prognostic factor. Many studies have reported about risk factors of coronary artery disease in Kawasaki disease. This study was designed to evaluate factors influencing coronary arterial involvement and to evaluate the effect of intravenous gammaglobulin (IVG) when admitted on the widely used criteria in Korea. Fiftyfour patients meeting the CDC criteria...
Case Report
A Case of Unilateral Absence of Pulmonary Artery
Joon Ho Bang, Sang Nyen Kim, Jong In Byun, Won Bae Lee, Byung Churl Lee, Kyong Su Lee, Sung Hoon Cho
Clin Exp Pediatr. 1992;35(6):873-878.   Published online June 15, 1992
A Unilateral Absence of Pulmonary Artery(UAPA), which develops occasionally as one of the associated anomaly in congenital cardiovascular defect like as tetralogy of Fallot, is rare anomaly as an isolated congenital defect. We have recently experienced a case of UAPA in a 9 years old boy, which was diagnosed by perfusion scan, digital subtraction angiography. So we report this case...
Original Article
A Case of Spindle Cell Thymoma with Spinal Cord Compression.
Ki Hyeok Lee, Dong Joo Nah, Jong In Byun, Sang Min Seong, Kyung Tai Whang, Eun Deok Chang, Young Hee Jee
Clin Exp Pediatr. 1988;31(9):1237-1242.   Published online September 30, 1988
We experienced a case who presented symptoms of spinal cord compression in association with posterior mediastinal thymoma. A 2-year old female patient was admitted to the hospital for evaluation of gait difficulty and motor weakness of legs which aggravated during two weeks prior to admission. General physical, mental status examination and cranial nerve functions were within normal limits. Diffuse moderate weakness of the lower extremities...