- Original Article
- Comparison of The Efficacy of the Fiberoptic Phototherapy and Conventional Phototherapy for Neonatal Hyperbilirubinemia
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Hye Jung Min, Gwi Sook Kim, Soo Kyung Lee, Il Kyung Kim, Ho Sung, Chang Hee Choi
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Clin Exp Pediatr. 1996;39(8):1076-1083. Published online August 15, 1996
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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... |
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- Case Report
- A Case of Combined Congenital Deficiency of Factor V and Factor VIII
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Kue Chang Cho, Soo Kyung Lee, Il Kyung Kim, Ho Sung, Chang Hee Choi
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Clin Exp Pediatr. 1996;39(8):1162-1167. Published online August 15, 1996
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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... |
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- Original Article
- Analysis of Radiologic Findings in Children with Urinary Tract Infection
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Won Suk Kuk, Il Kyung Kim, Ho Seong, Chang Hee Choi
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Clin Exp Pediatr. 1995;38(9):1242-1252. Published online September 15, 1995
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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... |
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- Case Report
- Two Cases of Conjoined twins
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Hyung Jo Jung, Swi Sook Kim, Il Kyung Kim, Ho Sung, Chang Hee Choi, Hyo Jin Lee
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Clin Exp Pediatr. 1995;38(9):1276-1282. Published online September 15, 1995
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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. |
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- Original Article
- Etretinate Induced Cardiovascular Malformations in Mouse Embryo
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Il Kyung Kim, Chang Sung Son, Young Chang Dockgo, Yong Hyuk Jeon
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Clin Exp Pediatr. 1995;38(10):1370-1377. Published online October 15, 1995
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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... |
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- Case Report
- A Case of Addison's Dlisease
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Baek Gil Lee, Hyang Sook Lee, Il Kyung Kim, Ho Sung, Chang Hee Choi
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Clin Exp Pediatr. 1992;35(7):989-994. Published online July 15, 1992
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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,... |
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- A Case of 7q-Syndrome
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Ja Hyun Park, Baek Gil Lee, Il Kyung Kim, Jung Sik Min, Chang Hee Choi
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Clin Exp Pediatr. 1992;35(3):422-427. Published online March 15, 1992
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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... |
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- Original Article
- A Case of Congenital Megakaryoblastic Leukemia Accompanied by Down Syndrome Which was Diagnosed by Autopsy Findings.
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Il Kyung Kim, Dong Beom lee, Jung Sik Min, Chang Hee Choi, Je Geun Chi
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Clin Exp Pediatr. 1989;32(2):262-269. Published online February 28, 1989
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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... |
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- Clinical Consideration on Pneumonia caused by Mycoplasma Pneumoniae in Children.
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Il Kyung Kim, Hyung Jin Kwon, Ho Seong, Chang Hee Choi
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Clin Exp Pediatr. 1989;32(1):1-10. Published online January 31, 1989
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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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