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Original Article
Clinical Study of 20 Pediatric Cases of HBs Antigenemia Associated Membranous Nephropathy.
Jae Seung Lee, Jung Hye Choi, Young Cherl Lee, Duk Jin Yun
Clin Exp Pediatr. 1984;27(8):760-765.   Published online August 31, 1984
A clinical study was done in 20 cases of HBs antigenemia associated membranous nephropathy admitted to the Department of Pediatrics, Yonsei University, College of Medicine, Severance hospital from Jan. 1979 to May 1984. The results are as follows; 1)The age distribution was from 2 years and 5 months to 14 years, and the mean age was 7 years and 10...
Laboratory and Clinical Study of Ceftizoxime Sodium (Epocelin(R)) in Infections of the Pediatric Age Group.
Keun Soo Lee, Hahng Lee, Jeh Hoon Shin, Kook Young Meng, Dae Keun Kim, Choon Won Kim
Clin Exp Pediatr. 1984;27(7):685-701.   Published online July 31, 1984
An in-vitro sensitivity of Ceftizoxime sodium (CZX), a third generation Cephalosporin, using Epocelin® (a product of Fujisawa Pharmaceutical Central Laboratory, Japan), was studied against various bacterial strains isolated from the children with infections hospitalized on the pediatric ward of Hanyang University Hospital during the period from February, 1983 up to June, 1983. And therapeutic responses were observed in 26 pediatric...
Case Report
A Case of Chronic Active Hepatitis with Vertical Transmission.
T H Son, T S Song, H J Park, M J Shin, J G Chi
Clin Exp Pediatr. 1984;27(2):164-169.   Published online February 28, 1984
We experienced a case of Chronic Active Hepatitis with vertical transmission in a 4-year-3-month old boy. Diagnosis of CAH was confirmed by histologic features of liver biopsy. The mode of infection in this case was suspected as vertical transmission by clinical history. His mother had acute hepatitis B in the last trimester of the pregnancy of this boy and had...
A Case of Osteogenesis Imperfecta Type II.
Chang Ick Lee, Young Ai Kim, Jung Joo Kim, Dong Hak Shin
Clin Exp Pediatr. 1984;27(1):93-97.   Published online January 31, 1984
Osteogenesis, imperfecta is an inherited disorder of connective tissue characterized by multiple fractures, blue sclerae, progressive deafness, loose jointedness, and skin. We experienced a case of Type I osteogenesis imperfecta in a 2 months old male infant who visited our hospital with chief complaints of generalized growth retardation, blue sclera and frequent fractures and deformities of limbs. With typical manifestation...
A Case Report Kostmann Syndrome.
Han Wook Yoo, Son Moon Shin, Hyo Seop Ahn, Yong Choi, Chang Yee Hong
Clin Exp Pediatr. 1983;26(3):284-288.   Published online March 31, 1983
Kostmann syndrome (Infantile genetic agranulocytosis), a disease characterized by recurrent infections leading to death in infancy, shows an agranulocytosis with variable monocytosis, eosinophilia in the peripheral blood, accompanied by the maturation arrest of the myelocytic series at the promyelocyte-myelocyte level. A 2 years 3 month old female patient with Kostmann syndrome is reported, who has suffered from recurrent infections since 1 month of age. During...
Two Case of Ginaotti-Crosti Syndrome.
Jae Ho Lee, Soon Ung Kang, Jeong Kee Seo, Hyo Seop Ahn, Kwng Wook Ko, Won Suk Kim
Clin Exp Pediatr. 1982;25(12):1289-1294.   Published online December 31, 1982
The Gianotti-Crosti syndrome is an. infrequently recognized disorder with distinctive clinical features. We have experienced two cases of Gianotti-Crosti syndrome diagnosed by clinical manifestation, laboratory data and histopathologic finding of skin. Case one; An 18-month-old girl was admitted to the pediatric ward with the chief complaint of erythematous rash. Its onset was preceded by an. upper respiratory tract infection. She had a wide spread erythematous...
A Case of Acardi's Syndrome.
Bok Lyun Park, Hee Jung Chung, Chang Joon Coe, Young Sook Seo
Clin Exp Pediatr. 1982;25(12):1285-1288.   Published online December 31, 1982
A case of Aicardi’s syndrome is experienced at the Department of Pediatrics, College of Medicine, Yonsei University recently. This patient was 50 days of female infant, who had infantile spasm, and her development was deteriorated recently. Her CT scan showed partial absence of corpus callosum and whose EEG was a pattern of modified hypsarrhythmia limited only on left hmisphere. She also had hemivertebra at...
Original Article
Clinical Study of Epilepsy in Children.
C J Coe, D K Han, K Y Lee, B S Kim
Clin Exp Pediatr. 1982;25(12):1234-1242.   Published online December 31, 1982
From November 1980 to June 1982, for 19 months, 636 cases of child epileptic patients were clinically investigated at Pediatric department of Yonsei Medical school, and obtained follo- wing results. 1. The epileptic patients was 4.4% of all the pediatric patients, visited or hospitalized during the same period of time. 2. Epilepsy was commoner in male child compare to female representing male to female ratio, 1.3:1. 3. The most common...
Case Report
A Case of Potter Syndrome.
Young Mi Hong, Hae Seung Kim, Jung Gon Kim, Keun Lee
Clin Exp Pediatr. 1982;25(11):1181-1184.   Published online November 30, 1982
In 1946 Potter described a series of 20 cases in infants in whom bilateral absence of the kidneys was associated with, hypoplasia of the lung and characteristic face. The main facial features she described were increased space between the eyes, a prominent fold which arises at inner canthus and sweeps downward and laterally below the eyes, unusual flattening of the nose, excessive recession of...
Original Article
Neurobehavioral Response of Newborn Infants Following Delivery by Normal Labor and Cesarean Section under General and Spinal Anesthesia.
Eun Ai Lee, Jung Hee Park, Yoon Ju Choi, Seung Ju Lee, Keun Lee
Clin Exp Pediatr. 1982;25(10):1032-1038.   Published online October 31, 1982
Scanlon*s Early Neonatal Neurobehavioral Scale was administered to 110 babies delivered by normal labor and cesarean section. Fifty of the mothers had normal vaginal delivery, thirty of the mothers were induced into general anesthesia with thiopental sodium and thirty of the mothers received spinal anesthe- sia with tetracaine before cesarean section. The Scanlon*s scale involves an assessment of the infant*s state of wekefulness, varius reflexes, his...
Case Report
A Case of Acute Fulminant Hepatitis Induced by Herpesvirus Hominus.
Hee Jung Chung, Ki Sup Chung, Duk Jin Yun, Jung Sook Kim
Clin Exp Pediatr. 1982;25(6):616-621.   Published online June 30, 1982
We have experienced a case with acute fulminant hepatitis induced by Herpesvirus homin-us. The patient, 11day-old male baby, was admitted with the chief complaints of poor sucking and jaundice for 3 days duration. On adimission, we performed bacterial cultures, liver function tests, blood coagulation test, TORCH study and routine hematologic studies. During these studies, bleeding tendency was n-oticed at the...
A Case of Cryptococcosis with Cutaneous Manifestation.
Jae Phil Kim, Hyun Ju Oh, Hyung Suk Byun, Kyung Ryong Huh, Chull Sohn
Clin Exp Pediatr. 1981;24(8):777-781.   Published online August 15, 1981
We experienced a case of cryptococcosis in a 13-year-old female who had been admitted to our hospital because of intermittent high fever and generalized lymphadenopathy accompanied by multiple nodular eruptions with erosions on the face, scalp, neck and back. The patient was treated under the impression of tuberculous lymphadenitis without any improvement. A surgical biopsy of the lymph node and...
A Case of Rt. Renal Agenesis Combined with Cryptorchism and Neuroblastoma.
Hee Jung Chung, Chul Lee, Pyung Kill Kim, Chang Jin Kim, Kwang Kill Lee, Yu Bok Lee, Ki Keun Oh
Clin Exp Pediatr. 1981;24(7):677-684.   Published online July 15, 1981
Congenital unilateral renal agenesis is a rare congenital anomaly. Furthermore, renal agenesis associated with neuroblastoma and cryptorchism is more rare in incidence. Recently we experieced a case of Rt. renal agenesis combined with cryptorchism and neuroblastoma. We diagnosed it with IVP and selective renal angiography and confirmed it with explolaparotomy and biopsy. We reviewed the literatures on renal agenesis, cryptorchism...
A Case of Congenital Generalized Lipodystrophy.
Woon Sik Kim, Kye Tae Kim, Don Hee Ahn, Keun Chan Sohn
Clin Exp Pediatr. 1981;24(2):173-180.   Published online February 15, 1981
A 4 year and 2 months old girl with peculiar appearance and abdominal protuberance was prese-nted. She was the 2nd full term product of a healthy, 37-year-old mother. Any history of neonatal problems couldn’t be elicited. At 1 month of age his mother began to notice loss of subcutaneous fat with prominent musculature. At 2 months of age he was...
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