• Search
  • Advanced Search

Search

  • HOME
  • Search
Original Article
Recent incidence of congenital heart disease in neonatal care unit of secondary medical center: a single center study
Seon Young Cho, Jin-Hee Oh, Jung Hyun Lee, Jae Young Lee, Soon Ju Lee, Ji Whan Han, Dae Kyun Koh, Chang Kyu Oh
Clin Exp Pediatr. 2012;55(7):232-237.   Published online July 17, 2012
Purpose

With feasibility in the diagnoses of congenital heart disease (CHD) in the antenatal period, we suspect changes have occurred in its incidence. No data have been reported about the current incidence of simple forms of CHD in Korea. We have attempted to assess the recent incidence and characteristics of CHD in the neonatal care unit of a secondary referral medical...

Isolation of Causative Microorganism and Antimicrobial Susceptibility Test in Impetigo Developed in the Past Four Years
Hyun Jeong Lee, Sang Jung Lee, Seog Jun Ha, Chang Kyu Oh, Jin Wou Kim
Clin Exp Pediatr. 2000;43(5):632-637.   Published online May 15, 2000
Purpose : Recently, Staphylococcus aureus has been reported as the principal microorganism isolated from impetigo, showing variable degrees of antimicrobial resistance. The aim of this work was to study the causative organism of impetigo the their antimicrobial susceptibility developed in impetigo in the past four years. Methods : We performed bacterial cultures and antimicrobial susceptibility tests in 73 patients with impetigo...
Case Report
A Case of Median Cleft Face Syndrome
Kyeong Hee Suh, Dae Chul Jeong, Jae Kyun Hur, Chang Kyu Oh
Clin Exp Pediatr. 2000;43(4):583-587.   Published online April 15, 2000
Median cleft face syndrome is diagnosed by two or more of the following anomalies : ocular hypertelorism, cranium bifidum occultum, median cleft nose, median cleft lip and median cleft premaxilla. The most consistent and prominent ocular finding associated with this syndrome is hypertelorism. We experienced a case of median cleft face syndrome which had orbital hypertelorism, cranium bifidum occultum, bifid...
A Case of Wolf-Hirschhorn Syndrome Resulting from Familial Translocation
So Yeon Yoon, Jae Kyun Hur, Dae Chul Jeong, Won Bae Lee, Chang Kyu Oh
Clin Exp Pediatr. 1999;42(8):1149-1153.   Published online August 15, 1999
Wolf-Hirschhorn syndrome is caused by a partial loss of the distal short arm of chromosome 4. Characteristic clinical features are severe growth retardation, mental retardation, seizures, congenital cardiac defects, urogenital abnormalities, microcephaly, hypertelorism, prominent glabella, cleft lip and palate and micrognathia. In 87% of cases, chromosome 4 deletion arises as a de novo event, whereas in the remaining cases it...
A Case of Infantile Acute Hemorrhagic Edema
Hyun Jeong Lee, Dong Won Lee, Si Yong Kim, Baik Kee Cho, Chang Kyu Oh
Clin Exp Pediatr. 1996;39(8):1168-1172.   Published online August 15, 1996
Infantile acute hemorrhagic edema(IAHE) is a variant of leukocytoclastic vasculitis which is characterized by painful edematous purpura of cockade pattern on the head and distal extremities. The lesions are limited to the skin and complete recovery occurs within 1 to 3 weeks. Recently, it is accepted as a separate entity from Henoch-Schönlein purpura. A nine month-old boy presented multiple cockade ecchymotic plaques and inflammatory...
Original Article
A Clinical Study of Congenital Hypertrophic Pyloric Stenosis.
Kwang Sun Park, Young Ki Park, Jong Wan Kim, Chang Kyu Oh, Mahn Kyoo Yang
Clin Exp Pediatr. 1989;32(1):27-33.   Published online January 31, 1989
We experienced 23 patients with congential hypertrophic pyloric stenosis from Dec. 1978 to Aug. 1987 The age and sex distribution, family and birth history, clinical symptoms with prognosis etc. were reviewed. The results were as follows. 1) Most of the patients (20 cases, 87%) represented symptoms within 6 weeks of age. 2) Male was predominated than female by the ratio of 19:4. 3) The first baby was...
Clinical Review of Tuberculous Meningitis in Children.
Hyung Kook Kim, Mi Aie Han, Jong Wan Kim, Chang Kyu Oh, Mahn Kyoo Yang
Clin Exp Pediatr. 1988;31(7):892-900.   Published online July 31, 1988
147 Cases of tuberculous meningitis who were admitted to the pediatric department of St. PauFs Hospital, Catholic University Medical College from Jan. 1972 to Dec. 1985 were reviewed clinically. The results were as follows 1) The sex ratio, male to female was 1.2:1 2) The age incidence was highest under the age of 1 and 84.4% of the petients were under the age of 6 years. 3) The seasonal...
Case Report
A Case of Lung Metastasis of Testicular Yolk Sac Tumor.
Ho Ju Yoon, Hyun Kyung Cho, Jung Sik Chun, Chang Kyu Oh, Mahn Kyoo Yang
Clin Exp Pediatr. 1982;25(12):1275-1279.   Published online December 31, 1982
First admission; A 4 year old male patient was admitted with progressive swelling and tenderness of left scrotum since birth. Left simple orchiectomy was performed. The histolo- gic finding was testicular yolk sac tumor. Second admission; 2 years later. The patient was readmitted with migrating pain and limitation of motion of lower extremities. Lung metastasis (LLL extending to lingular lobe) was appeared. During chemotherapy, he...
Original Article
A Clinical Observation on Acute Bronchiolitis.
Jong Man Lee, Won Ik Lee, Jong Seung Kim, Chang Kyu Oh
Clin Exp Pediatr. 1982;25(12):1218-1224.   Published online December 31, 1982
A clincial study of 289 cases of acute bronchiolitis, which were admitted to the pediatric department of St. Paul’s Hospital during the period of 6 years from January 1975 to December 1980 was reviewed. The results were as follows: 1. Male was predominant, and male to female ratio was 2.3 : 1. 2. The highest incidence (72.3%) was in infants below the age of 6 months and...
Case Report
A Case Of Choledochal Cyst In A Neonate.
Jong Man Lee, In Kyung Sung, Jong Seung Kim, Chang Kyu Oh
Clin Exp Pediatr. 1982;25(10):1068-1072.   Published online October 31, 1982
Congenital choledochal cyst is a rare disease, especially in fetal life and early infancy age. Our case was a 66 days old female baby who had the symptoms of jaundice, clay-colored stool, intermittent vomiting since birth and abdominal distension. Final diagnosis was choledochal cyst with neonatal hepatitis. An early accurate preoperative diagnosis has been associated with a marked decrease in the mortality. Roux-en-Y choledochocystojejunostomy was done. We...
A Case of Patent Urachus.
Jong Wan Kim, Hack Ki Kim, Chung Sik Chun, Chang Kyu Oh, Mahn Kyoo Yang
Clin Exp Pediatr. 1982;25(3):295-299.   Published online March 31, 1982
Pateat urachus is a uncommon disease and it has a good prognosis if there is no combired major anomaly and evidence of malignancy. This paper presents one case of patent urachus which was found and removed surgically during the neonatal period. A brief review of related literatures is also presented.
A case of Aplastic Anemia following Hepatitis.
Yong Eun Chung, In Kyung Sung, Chung Sik Chun, Chang Kyu Oh, Mahn Kyoo Yang
Clin Exp Pediatr. 1980;23(8):670-673.   Published online August 15, 1980
Aplastic anemia following hepatitis is uncommon disease and it has a poor prognosis. Recently authors expirienced a case of aplastic anemia following hepatitis in 13-year-old boy. He was admitted due to jaundice and ecchymosis for 1 month. During admission, pancytopenia developed and there was marked hypocellularity of all elements in bone marrow examination. His clinical course was not improved in...
Original Article
A Clinical and Statistical Observation on the Idiopathic Neonatal Hyperbilirubinemia.
Eun Suk Kim, chang kyu Oh, Jung Il Kim, Mahn Kyoo Yang, jin sub lee
Clin Exp Pediatr. 1980;23(2):118-124.   Published online February 15, 1980
Clinical and statistical observations were performed on 97 newborn infants who were admitted to newborn nursery of St. Paul's Hospital from September, 1978 to August, 1979 with the diagnosis of idiopathic neontal hyperbilirubinemia and the following results were obtained. 1. The highest monthly incidence was seen in March with 19 cases(19.2%). 2. The peak gestational age and birth weight were...