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Original Article
Organic Acidemias in Korea - Three Years Experience of Organic Acid Analysis -
You Kyoung Choi, Eung Seok Kim, Eun Joo Bae, Won Il Park, Kyung Ja Lee, Hong Jin Lee
Clin Exp Pediatr. 2002;45(11):1346-1358.   Published online November 15, 2002
Purpose : We have done this retrospective study to know the relative incidences and clinical manifestations of organic acidopathies in Korea. Methods : The results of quantitative organic acid analysis of 1,125 samples of 712 patients, referred from Jul. 1997 to Jun. 2000, were analyzed retrospectively according to four age groups (-2 mon, 3 mon-2 year, 3 years-12 years, over...
Case Report
A Case of Dominantly Inherited β Thalassemia Due to Hb Dieppe
You Kyoung Choi, Hong Jin Lee, Won Il Park, Kyung Ja Lee, Sung Ha Kang, Ji Yeon Kim, Sung Sup Park
Clin Exp Pediatr. 2002;45(5):659-663.   Published online May 15, 2002
β thalassemias are usually transmitted as autosomal recessive traits. However, some dominant forms of β thalassemia have been identified in individuals who have inherited a single copy of an abnormal β globin gene. Thalassemia intermedia with mild anemia, jaundice, and splenomegaly has been observed in these patients. Electrophoresis has shown elevated Hemoglobin(Hb) A2 and Hb F levels. In particular, there...
A Case of Maple Syrup Urine Disease Controlled by Peritoneal Dialysis and Diet
Ju Wan Kim, June Huh, Won Il Park, Kyung Ja Lee, Hong Jin Lee
Clin Exp Pediatr. 2001;44(1):94-98.   Published online January 15, 2001
Maple syrup urine disease is an autosomal recessive disease caused by a deficiency of the branched-chain α-ketoacid dehydrogenase complex. The disease is often suspected because of the peculiar odor of maple syrup in urine. Maple syrup urine disease is usually confirmed by amino acid analysis and urine organic acid analysis showing marked elevations of leucine, isoleucine, valine, and respective ketoacids in...
Erythrocyte Band 7 Integral Protein Defectin Congenital Hemolytic Anemia: Hereditary Stomatocytosis
Chang Seoup Sim, Sang Joo Han, Hong Jin Lee, Woo Ill Park, Kyung Ja Lee, So Young Chung, Sechan Woo, Eui Yul Choi
Clin Exp Pediatr. 1997;40(2):260-264.   Published online February 15, 1997
Hereditary stomatocytosis is a rare congenital hemolytic anemia, named after mouth shaped or stomatocytic erythrocyte morphology. In this report, we present a case of a hereditary stomatocytosis in a 1 month old boy. During the initial identification process, we overlooked the morphology of the RBC in peripheral blood smear and tentatively diagnosed it to be a hereditary spherocytosis case. In order to...
Original Article
Age Related Ca, Phosphorus, Uric acid concentration in Serum & Urine and Ca/Cr ratio, Cua/Ccr & TRP
Jah In Kim, Sang Joo Han, Hong Jin Lee, Won Il Park, Kyung Ja Lee
Clin Exp Pediatr. 1996;39(10):1405-1413.   Published online October 15, 1996
Purpose : There are many methods for the evaluation of the renal function. The proximal tubule of the nephrons have a role of reabsorption of the materials such as water, electrolytes, glucose, amino acids, and small molecular weight protein through the glomerular filtration. Therefore if abnormality is in the proximal tubule, these materials can be changed both in serum & urine. It is very...
A Clinical Study of Benign Epilepsy of Childhood with Centrotemporal Spikes
Byung Il Lee, Sang Ju Han, Hong Jin Lee, Won Il Park, Kyung Ja Lee
Clin Exp Pediatr. 1994;37(9):1251-1256.   Published online September 15, 1994
Benign epilepsy of childhood with centrotemporal spikes(BECCT) is an electroclinical syndrome characterized by noctural seizure that remit spontaneouly before adulthood, and belong to idiopathic age and location related epilepsies. We reviewed the medical records to analyse the seizure pattern, and also inspect the EEG recording to identify topography of the epileptiform discharge of 24 patient who met the following criteria: 1)presence...
Clinical Observation of urinary Tract Anomalies
In Hee Jung, Hong Jin Lee, Sang Joo Han, Won Il Park, Kyung Ja Lee
Clin Exp Pediatr. 1994;37(8):1092-1096.   Published online August 15, 1994
Urinary tract anomaly is the most common anomaly in childhood. We reviewed medical records of 45 patients who were confirmed urinary tract anomalies on radiologic studies as Chuncheon Sacred Hospital, from Dec. 1984 to Sep. 1992. We analyzed incidence and clinical characteristics of urinary tract anomalies. The results obtained were as follows: 1) The age distrtibution were: 17 cases (37.8%) under...
Effect of Different Levels of the Dietary Protein on Long Term Prognosis of Experimental Renal Damage
Choon Haeng Lee, Sang Joo Han, Hong Jin Lee, Won Il Park, Kyung Ja Lee, Young Eui Park, Min Chul Lee, Tae Heon Yoon
Clin Exp Pediatr. 1993;36(6):820-829.   Published online June 15, 1993
We examined the effect of various levels of dietary protein on long term prognosis of Adriamycinephropathy of S-D rat, fed with high protein(30%), intermediately low(10%), and strictly low(5%) protein diet for 15 weeks 1) In rats fed with strictly low protein diets(5%), proteinuria and serum creatinine decreased and creatinine clearance and histological changes were relatively well preserved. But hypoproteinmia and weight...
Case Report
A Case of Stein-Leventhal Syndrome with Severe Obesity
Kyeong Sang Kim, In Hee Jung, Hong Jin Lee, Won Il Park, Kyung Ja Lee
Clin Exp Pediatr. 1992;35(8):1164-1168.   Published online August 15, 1992
We experienced a extremely rare case of Stein-Leventhal Syndrome in 7 year-old female patient. Her chief complaints was severe obesity. We performed specific radiologic and hormonal studies. Diagnosis was suspected by pelvic sono and CT. We performed vertical gastroplasty with Taplon bandage for morbid obesity. A brief review of related literature was made.
Original Article
HDL Cholesterol, Copper, Ceruloplasmin, Zinc, Iron Values of the Blood in Newborn
Kyeong Sang Kim, Chun Hang Lee, Hong Jin Lee, Won Ill Park, Kyung Ja Lee, Tae Hyon Yoon, Won Chan Tae
Clin Exp Pediatr. 1992;35(8):1096-1101.   Published online August 15, 1992
HDL choleaterol, copper, ceruloplasmin, zinc, and iron values of the blood of 85 newborns delivered at hallym University hospital from September, 1989 to February, 1991 were analysed. The results were as follows: 1) The mean value of HDL cholesterol in 50 normal newborns was 31.37¡¾9.47mg/dl, that of copper 80.54¡¾17.54ug/dl, that of ceruloplasmin 11.34¡¾6.37mg/dl, that of zinc 92.81¡¾79.74ug/dl, that of iron 198.98¡¾86.07 ug/dl. 2)...
A Case of Lamellar Ichthyosis.
Yeon Seung Lim, Sang Joo Han, Won Il Park, Kyung Ja Lee
Clin Exp Pediatr. 1990;33(7):1018-1023.   Published online July 31, 1990
We observed a case of lamellar ichthyosis who was 4 day-old boy with the chief complaints of poor feeding, exessive lamellated scale covering entire body. Diagnosis of lamellar ichthyosis was estab- lished by clinical features and histopathological study. A brief review of literature was made.
A Case of Congenital Cysitic Adenomatoid Malformation of Lung.
Youe Kawn Kim, Deuk Hwan Jun, Bae Young Kim, Won Il Park, Kyung Ja Lee
Clin Exp Pediatr. 1990;33(2):225-228.   Published online February 28, 1990
Congenital cystic adenomatoid malformation is a rare variant of pulmonary cystic disease char- acterized by a mass of cysts lined by proliferating bronchial or cuboidal epithelium. The onset of symptoms, which are cyanosis, and tachypnea, usually occurs during the first week of life. We have experienced a case of congenital cystic adenomatoid malformation in a 9 month-old female. The diagnosis was mady by chest...
One Case of Leptospirosis.
Sang Joo Han, Jung Hyeun Park, Kyung Ja Lee, Woo Kap Chung
Clin Exp Pediatr. 1990;33(1):107-110.   Published online January 31, 1990
Leptospirosis is a zoonosis distributed worldwide. Ifs caused by spirochetes of the genus leptospira and charaterized by systemic and protean clinical manifestation. On August 1981, a diagnosis of this disease was made by a serologic test. Thereafter many cases were reported in adults, but there are no published reports in children. This report deals with one case of leptospirosis in children diagnosed by clinical...
A Case of Rickettsia Typhi.
Deuk Hwan Jun, Sang Joo Han, Bae Young Kim, Won Il Park, Kyung Ja Lee
Clin Exp Pediatr. 1989;32(12):1736-1739.   Published online December 31, 1989
We experienced one case of rickettsia typhi. This 6 years old male was admitted to Sacred Heart Hospital because of fever, Headache and myalgia for 10 days. Physical examination showed him to have injection of throat, dry lips with no skin rash. In the laboratory findings, the CSF showed cell count 22/mm3and suger and protein were with in normal limit. In peripheral blood smear, moderate left...
Case Report
A Case of Prune Belly Syndrome.
Gyu Ho Lim, Kyung Ja Lee, Woo Kap Chung
Clin Exp Pediatr. 1986;29(8):918-923.   Published online August 31, 1986
Prune belly syndrome is a very rare congenital anomaly characterized by congenital deficiency of the abdominal muscle wall and wrinkled irregular skin, prune like in appearance. It has been referred to as triad syndrome because three major features are seen in most cases: deficiency of the abdominal muscle wall, hydroureter and hydronephrosis, and cryptochidism. We report a rare case of...
Original Article
The Clinical Statistical observation of Congenital Syphilis
Buem Soo Roh, Kyung Ja Lee, Yong II Lee, Sang Jhoo Lee
Clin Exp Pediatr. 1971;14(3):175-180.   Published online March 31, 1971
The authors observed 31 cases of congenital syphilis in the newborn and infants treated at pediatric ward of Han-Il Hospital during the period from Jan. 1965 to Feb. 1671. The results are as follows. 1)The number of patients was 31 cases, 23 in male and 8 in female. 2)The incidence of congenital syphilis in the newborn infants who were delivered...
Case Report
An Autopsy Case of Situs Inversus Viscerum Totalis
Kyung Ja Lee, Jong Hyuk Lee, Yong Kil Lee, Sang Jhoo Lee, Je G. Chi, Geung Hwan Ahn
Clin Exp Pediatr. 1969;12(12):715-720.   Published online December 31, 1969
An 2. 7 kg weighing male baby was born with a large pedunculated mass in the occipital area of the head. The baby expired on 21st day after birth, due probably to infected cephalocele with diarrheal disorder. Postmortem examination revealed the following: All thoraco-abdominal viscera and vessels were in the mirror-image position of the normal. The heart was in the...
Two Cases of Spontaneous Fractures in Miliary Tuberculosis and Tuberculous Meningitis
Chang Hyup Kim, Jong Hyuck Lee, Kyung Ja Lee, Sang Jhoo Lee
Clin Exp Pediatr. 1968;11(2):91-94.   Published online February 28, 1968
Only few cases describing spontaneous fractures in tuberculous meningitis were reported in the literatures. Recently, we experienced two such cases, who daring their treatment for miliary tuberculosis and tuberculous meningitis developed spontaneous fractures of the lower extremities. Case 1: A 3 year and 4 month old Korean boy was admitted to Hanil Hospital on September 8,1966, with chief complaints of...
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