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Original Article
Clinical significance of follow-up laboratory tests, performed at 6 weeks after the onset of Kawasaki disease
Il Ji Oh, Kyung Hee Moon, Myung Eun Hong, Yeon Soon Kim, Chang Woo Lee, Hyang Suk Yoon
Clin Exp Pediatr. 2006;49(6):672-676.   Published online June 15, 2006
Purpose : Low dose aspirin is used due to its antiplatelet effect for the subacute phase of Kawasaki disease(KD). It is usually used for 6-8 weeks, then various hematologic laboratory tests and follow up echocardiography for evaluating coronary abnormalities are performed. Our review investigated the usefulness of various follow up laboratory tests performed at 6 weeks after the onset of...
Case Report
3 Cases of Congenital Hypothyroidism.
Chul Hwan Park, Moo Young Oh, Tae Gyu Hwang, Soon Yong Lee, Yeon Soon Kim
Clin Exp Pediatr. 1987;30(3):320-326.   Published online March 31, 1987
We observed 3 cases of congenital hypothyroidism. A 43-day-old girl, a 372-month-old boy and a 5-year-old girl were presented. The causes were thyroid agenesis of case I, defective TSH receptor (suspect) of case II and undetermined in case III respectively. The diagnosis was made by clinical manifestations, thyroid function test, A brief review of literatures was made.
A Case of Combined Esophageal Atresia and Duodenal Atresia.
Ju Yeong Seo, Cheol Lee, Woo Yeong Chung, Soon Yong Lee, Yeon Soon Kim
Clin Exp Pediatr. 1985;28(9):912-915.   Published online September 30, 1985
We experienced a case of combined esophageal atresia without tracheoesophageal fistula and duodenal atresia. Choanal Atresia was also associated. The diagnosis was confirmed by prenatal ultrasonography, abdominal radiography and autopsy. A review of literatures was also presented briefly.
A Case of Congenital Monocytic Leukemia.
Woo Yeong Chung, Eue Bon Koo, Hak Jun Ko, Tai Gyu Whang, Soon Yong Lee, Yeon Soon Kim
Clin Exp Pediatr. 1984;27(10):1022-1027.   Published online October 31, 1984
We experienced a case of congenital monocytic leukemia in a 25 day old female newborn infant. She was admitted because of petechiae, abdominal distension and skin nodules scattered on. whole body. Diagnosis was confirmed with findings of CBC, bone marrow aspiration and cytochemistry. A review of literatures was also presented.
A Case of Neurofibromatosis associated with Pseudoarthrosis of the Ulna.
Ju Yeong Seo, Woo Yeong Chung, Soon Yong Lee, Kil Hyun Kim, Yeon Soon Kim
Clin Exp Pediatr. 1984;27(5):516-520.   Published online May 31, 1984
We experienced a case of neurofibromatosis associated with pseudoarthrosis of the ulna in a 5-year-old boy. He had multiple cafe-au-lait spots, neurofibromas, and macrocranium with positive family history. A review of literatures was also presented briefly.
A Case of Hepatic Hemangioendothelioma.
Ki Tae Kim, Heon Kyung Lee, Soon Yong Lee, Young Sik Park, Kil Hyun Kim, Yeon Soon Kim
Clin Exp Pediatr. 1984;27(4):395-400.   Published online April 30, 1984
We experienced a case of hepatic hemangioendothelioma in a 21-day-old girl who had a large mass in the left upper quadrant of abdomen. The diagnosis was confirmed by laparatomy and histological finding. A review of the related literatures was also made.
A Case of Patent Urachus.
Heon Kyung Lee, Ki Tae Kim, Woo Yung Chung, Soon Yong Lee, Yung Sik Park, Yeon Soon Kim
Clin Exp Pediatr. 1984;27(1):89-92.   Published online January 31, 1984
We present a case of patent urachus in a newborn male baby with the symptom of a leakage of urine from the umbilicus. Diagnosis was made radiologically and it was surgically removed successfully. A brief review of related literatures is also presented.
Two Cases of Patent Omphalomesenteric Duct.
Heon Kyung Lee, Ki Tae Kim, Woo Yeong Cheong, Soon Yong Lee, Young Sik Park, Yeon Soon Kim
Clin Exp Pediatr. 1983;26(10):1013-1017.   Published online October 31, 1983
Patent omphalomesenteric duct occurs when there is primary failure of luminal closure of vitellointestinal duct during the fetal life, and it makes an abnormal communication between the intestine and the umbilicus. We presented two cases of patent omphalomesenteric duct in the neonatal period. Diagnosis was confirmed by radiological examination and surgery. Surgical removal was done successfully. A brief review of related literature was also presented.
A Case of Gaucher'S Disease In Identical Twins.
Woo Yeong Chung, Ki Tae Kim, Heon Kyung Lee, Soon Yong Lee, Young Sik Park, Yeon Soon Kim, Soon Ho Kim, Eun Yup Lee
Clin Exp Pediatr. 1983;26(6):598-605.   Published online June 30, 1983
We experienced a case of Gaucher’s disease of adult type in 3 year 8 month old male who was one of identical twins with family history of splenomegaly in his two siblings. Diagnosis was based on clinical pictures such as marked hepatosplenomegaly with anemia and characteristic pathologic findings of liver and spleen. There were no specific complications after splenectomy until now. Review of literatures was...
Original Article
The Effect of Blue Light and White Light, Continous and Intermittent Phototherapy in the Treatment of Jaundice for the Low Birth Weight Infants.
Ki Tae Kim, Heon Kyung Lee, Woo Yeong Chung, Soon Youg Lee, Yeon Soon Kim
Clin Exp Pediatr. 1983;26(4):299-303.   Published online April 30, 1983
The effect of phototherapy was studied between blue and white lights, and continuous and intermittent regimens in the treatment of jaundice for the low birth weights at Busan Children’s Hospital from October, 1981 to March, 1982. The results were as following: 1) The duration of phototherapy necessary to reduce serum bilirubin level below 8 mg/dl were 58.9 hours with blue light, and 102.3 hours with white...