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Case Report
A Case of Combined Congenital Deficiency of Factor V and Factor VIII
Kue Chang Cho, Soo Kyung Lee, Il Kyung Kim, Ho Sung, Chang Hee Choi
Clin Exp Pediatr. 1996;39(8):1162-1167.   Published online August 15, 1996
Hemorrhagic disease of newborn by combined blood clotting factor deficiencies is very rare. Combined deficiency of factor V and factor VIII is the most common form among these cases, and inherited by autosomal recessive trait. Clinical findings are easy bruising, posttraumatic bleeding and bleeding after tooth extractions, and the main laboratory findings are prolonged partial thromboplastin time (PTT) and prothrombin time (PT) that are...
Original Article
Comparison of The Efficacy of the Fiberoptic Phototherapy and Conventional Phototherapy for Neonatal Hyperbilirubinemia
Hye Jung Min, Gwi Sook Kim, Soo Kyung Lee, Il Kyung Kim, Ho Sung, Chang Hee Choi
Clin Exp Pediatr. 1996;39(8):1076-1083.   Published online August 15, 1996
Purpose : We performed this study in order to compare the feasibility and efficacy of the fiberoptic phototherapy with conventional phototherapy and double phototherapy with single phototherapy for the treatment of neonatal hyperbilirubinemia while watching for any possible side effects of the system. Methods : During the period of February 1994 till June 1995, randomized controlled study was performed. 130 healthy term infants with non-hemolytic...
Etretinate Induced Cardiovascular Malformations in Mouse Embryo
Il Kyung Kim, Chang Sung Son, Young Chang Dockgo, Yong Hyuk Jeon
Clin Exp Pediatr. 1995;38(10):1370-1377.   Published online October 15, 1995
Purpose : Etretinate(Tigason? is an aromatic retinoid currently in therapeutic use for psoriasis but studies have shown that it is a potent teratogen in human and in experimental animal. So we carried this study to observe teratogenic effects of etretinate and to search a possibility of etretinate for using as an experimental model to induce cardiovascular malformation. Methods : In order...
Case Report
Two Cases of Conjoined twins
Hyung Jo Jung, Swi Sook Kim, Il Kyung Kim, Ho Sung, Chang Hee Choi, Hyo Jin Lee
Clin Exp Pediatr. 1995;38(9):1276-1282.   Published online September 15, 1995
Conjoined twins are known to be very rare congenital malformations and may be viewedas examples of incomplete twining. Because of their associated anomalies, particularly of cardiovascular system, they usually survive only short postnatal period. We have experienced 2 cases of conjoined twins. One case of dicephalus dipus dibrachius and another case of thoracopagus are presented with brief review of literature.
Original Article
Analysis of Radiologic Findings in Children with Urinary Tract Infection
Won Suk Kuk, Il Kyung Kim, Ho Seong, Chang Hee Choi
Clin Exp Pediatr. 1995;38(9):1242-1252.   Published online September 15, 1995
Purpose : Because some patients with urinary tract infection (UTI) may combine vesicoureteral reflux and progress to reflux nephropathy, the early diagnosis and treatment of UTI are important. We have performed this study to recognize the meaning of the radiologic examination centering around technetium 99m- labelled dimercaptosuccinic acid renal scan(DMSA scan) in pediatric UTI patients. Methods : We have studied 55...
Case Report
A Case of Addison's Dlisease
Baek Gil Lee, Hyang Sook Lee, Il Kyung Kim, Ho Sung, Chang Hee Choi
Clin Exp Pediatr. 1992;35(7):989-994.   Published online July 15, 1992
A 14-year-old Korean boy with Addison's disease probably of tuberculosis origin is presented with a brief review of the literature. The patient was admitted to our hospital on July, 23th, 1990, because of dark brown pigmentation of the skin, mucous membrane and nail beds. On physical examination, he was moderately developed, relatively poorly nourished. Skin and mucous membranes were diffusely dark brown,...
A Case of 7q-Syndrome
Ja Hyun Park, Baek Gil Lee, Il Kyung Kim, Jung Sik Min, Chang Hee Choi
Clin Exp Pediatr. 1992;35(3):422-427.   Published online March 15, 1992
7q-syndrome, although rare, is a well defined syndroime which usually arises de novo. Characteristic clinical features include severe growth and metal retardation, microcephaly, low birth weight, broad nasal bridge with bulbous nasal tip, large, low set ears and genital anomalies. We experienced a male newborn with clinical features suggestive of chromosomal anomaly which was confirmed to be a 7q-(q32-qter) syndrome...
Original Article
A Case of Congenital Megakaryoblastic Leukemia Accompanied by Down Syndrome Which was Diagnosed by Autopsy Findings.
Il Kyung Kim, Dong Beom lee, Jung Sik Min, Chang Hee Choi, Je Geun Chi
Clin Exp Pediatr. 1989;32(2):262-269.   Published online February 28, 1989
Many cases of acute megakaryonlastic leukemia have been reported in childhood or adults, but congenital form or the cases occuring in neonatal period is very rare throughout the world. In Korea only one case was reported previously by Chung et al in 1987. The authors experienced a case of congenital megakaryoblastic leukemia accompanied by Down' s syndrome, which was confirmed by autopsy and positive...
Clinical Consideration on Pneumonia caused by Mycoplasma Pneumoniae in Children.
Il Kyung Kim, Hyung Jin Kwon, Ho Seong, Chang Hee Choi
Clin Exp Pediatr. 1989;32(1):1-10.   Published online January 31, 1989
A retrospective analysis of clinical findings in 63 patients above 2 years of age who were admitted to our hospital due to pneumonia caused by Mycoplasma pneumoniae from July, 1986 to June, 1987 was performed. The results obtained were as follows: 1) The number of patients showing positive reaction to cold agglutinin test (above 1:64) were 59 (55. 7%) among 106 total pneumonia cases. 2) The...
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