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Case Report
Morquio's Syndrome Accompanied by Respiratory Failure
Jun Hur, Hyeon Jeong Lee, Jeong Hwa Whang, Hee Jin Kim, Chan Yung Kim
Clin Exp Pediatr. 1997;40(7):1015-1020.   Published online July 15, 1997
Authors experienced a case of Morquio’s syndrome accompanied by respiratory failure in a aged fifteen year old boy. Patient showed normal intelligence, but stunted growth with short trunk and unproportionately large head, pectus carinatum, kyposcoliosis, muscular weakness, paralysis and genu valgum. No other member of family was affected with this syndrome. There were radiological findings of subluxation between first and second cervical vertevrae, central beaking with...
A Case of Congenitial Pyloric Atresia
Hyeon Jeong Lee, Jun Hoe, Jeong Hwa Whang, Gae Soon Yeo, Hee Jin Kim, Chan Yung Kim, Jun Hyeon Kim
Clin Exp Pediatr. 1995;38(12):1713-1717.   Published online December 15, 1995
In the newborn, a complete occlusion of the pyloric outlet is an extremely rare event. Authors experienced a case of pyloric atresia in a 2-day old boy, Who was admitted because of nonbilious vomiting. The plain radiograph of the abdomen showed gas in the huge stomach, but no gas noted distally. At operation, 3 days after birth, the pylorus was atretic...
Two Cases of Familial β-Thalassemia Minor
Jeong Hwa Hwang, Hyeon Jeong Lee, Jun Hur, Gae Soon Yeo, Hee Jin Kim, Chan Yung Kim, Tae Jun Yun
Clin Exp Pediatr. 1995;38(6):867-871.   Published online June 15, 1995
The β-thalassemia minor is a hereditary microcytic, hypochromic anemia characterized by decerased producion of β-globin polypeptide chain. The β-thalassemia minor should be clinically differentiated from iron deficiency anemia. The thalassemia are common in the Medeterranean region, the Middle Ease, the Africa, Indea, and Thailand, but rare in Korea. The authors experienced two cases of familial β-thalassemia minor 4-year 7-month-old female patient and...
Original Article
The Effect of Long-Term Corticosteroid Treatment on Height Velocity in Childhood
Byung Mun Lee, Chan Yung Kim
Clin Exp Pediatr. 1993;36(2):185-194.   Published online February 15, 1993
The auther analysed 29 patients who were treated with prednisolone, including nephrotic syndrome(13 cases). Acute leukemia (10 cases), bronchial asthma(2 cases), juvenile rheumatoid arthritis(2 cases) and ulcerative colitis(1 cases) patients in childhood, after remission induction, prolonged alternate or interrupted treatment was used. The auther observed patterns of height velocity of these patients from 1.6 to 10.3 years. The results were as...
A Study on the Atlantoaxial Instability in Children with Down syndrome
Sa Young Kim, Chan Yung Kim
Clin Exp Pediatr. 1993;36(2):179-184.   Published online February 15, 1993
To evaluate the atlantoaxial instability in children with Down syndrome, the authors analyzed the 97 children with Down syndrome attending to 2 schools for handicaped children in Pusan. The results of study were as follows; 1) The incidence of atlantoaxial instability in 97 individuals with Down syndrome was 8(8.3%) in neutral position and in 10(10.3%) in flexion, respectively. 2) The mean atlantoaxial gap...
Analysis of Foreign Body in the Children's Airway and Follow-up Study
Jae Hong Park, Chan Yung Kim
Clin Exp Pediatr. 1993;36(2):169-178.   Published online February 15, 1993
The autor analysed foreign body in the airway, divided into two groups vegetable foreign body group(VFBG) and non-vegetable foreign body group(N-VFBG), according to the nature, in 88 patients aged from 5 months to 15years who were diagnosed and treated under ventilating bronchos copy at Department of Pediatrics and Otolaryngology, Pusan National University Hospital from 1980 to 1990. Of the 88...
Case Report
A Case of Distal Type of Renal Tubular Acidosis in a Neonate
Sung Sub Shim, Young Joon Kim, Jae Hong Park, Soo Yung Kim, Chan Yung Kim
Clin Exp Pediatr. 1992;35(7):1014-1018.   Published online July 15, 1992
A female infant at 38 days of age was admitted to pediatric department of Pusan National University hospital due to dehydration, weight loss, vomiting, polyuria. Physical exmination at the time of admission revealed a slightly anemic, moderately dehydrated, dwarfed female infant in no acute distress. Laboratory studies on admission revealed hypokalemic, hyperchloremic metablic acidosis with normal anion gap and persistent...
Original Article
A case of benign recurrent intrahepatic cholestasis.
Jae Hong Park, Sung Sub Sim, Soo Young Kim, Hee Joo Jeon, Chan Yung Kim
Clin Exp Pediatr. 1991;34(12):1745-1752.   Published online December 31, 1991
The clinical picture of beingn recurrent intrahepatic cholestasis (BRIC) consists of multiple epi- sodes of cholestatic jaundice without extrahepatic bile duct obstruction. Since first description by Summerskill and Walshe in 1959, almost 100 patients with BRIC have been described. The mechanism involved in the initiation and perpetution of an episode of cholestasis are unknown. Altered bile acid metabolism has been proposed to play a...
Brain CT and clinical finding in tuberlous meningitis.
Moon Chan Kim, Chan Yung Kim
Clin Exp Pediatr. 1991;34(10):1391-1399.   Published online October 31, 1991
In this study, we evaluated clinical symptoms, neurologic findings, CSF examinations and prognosis of patients who were diagnosed to have tuberculous meningitis at Pusan National University Hospital and Gospel Hospital from march, 1983 to december, 1989. 1) Mean age was 3 years and 8 months and the percentage of patients under 6 years old was 71.9%. The male to female ration was 2.2:1. 2) Fever and vomiting...
Clinical observation on juvenile theumatoid arthritis.
Sung Sub Shim, Chan Yung Kim
Clin Exp Pediatr. 1991;34(8):1123-1131.   Published online August 31, 1991
The authors analyzed the clinical features, and the therapeutic responses in 29 patients with juvenile rheumatoid arthritis who were diagnosed and followed at Department of Pediatrics, Pusan National University Hospital from 1980. 1 to 1990. 6. The following results were obtained 1) Of the total 29 patients, 12cases (41.4%) were pauciarticular type II and 7cases (24.2%) were polyarticular RF(—) type. Seventeen cases (58.7%) were 8-11 yrs...
Clinical Study of Fulminant Hepatitis in Childhood.
Se Wook Oh, Chan Yung Kim
Clin Exp Pediatr. 1990;33(7):923-931.   Published online July 31, 1990
Twenty one cases of childhood fulminant hepatitis admitted to Pediatric department of Pusan National University Hospital form Jan. 1979 to Sep. 1989 were analysed. The results were as follows; 1) Age distribution was from 8 months to 13 yerars old and 66.7% of the patients were 2 to 9 year old of age. In sex ratio, male to female was 1,6:1. 2) Presumable etiologic factors were HBV...
A Study on the Pre-and Post-operative Growth Status of Children with Ventricular Septal Defect.
Kyung Hwan Kim, Chan Yung Kim
Clin Exp Pediatr. 1990;33(4):463-471.   Published online April 30, 1990
To evaluate the growth status of Congenital Heart Disease, we analyzed the 69 children with Ventricular Septal Defect who were admitted to Pediatric department and Chest Surgery department, Pusan National University Hospital from January, 1986 to June, 1987. The result of study were as follows: 1) This group was composed of 69 consecutive operation on children with ventricular septal defect. The sex distribution chanced to be...
Clinical Evaluation on Newborn of Teenage Pregnancy.
Man Cheol Ha, Chan Yung Kim
Clin Exp Pediatr. 1990;33(3):306-314.   Published online March 31, 1990
The authors have analysed the clinical characteristics of 117 cases of teenage pregnancy and their 122 newborn cases who were visited Pusan National University Hospital and Hae Sung Hospital from January 1982 to August 1988. The results were summarized as follows; 1) The youngest teenage mother was 14 years old, and below 17 years old was 28.2% and the remainder were between 18 and 19 years...
A Clinical Study of Infants and Children with Urinary Tract Infection.
Hyoung Doo Lee, Chan Yung Kim
Clin Exp Pediatr. 1989;32(12):1706-1714.   Published online December 31, 1989
Clinical, bacteriologic and radiologic studies were performed in 63 infants and children with urinary tract infection who were admitted to Department of Padiatrics, Pusan National University Hospital from March 1982 to February 1988. The results were summarized as follows: 1) UTI was more prevalent in infancy and early childhood (71.4%). Sex distribution was similar in all age group, and male was more prevalent in infancy and...
A Study on Periphral T Cell Subsets in Asymptomatic HBsAg Carriers and Children with Chronic Hepatitis B and Hepatitis B vaccine Inoculated Infants.
Hee Joo Jeon, Chan Yung Kim
Clin Exp Pediatr. 1989;32(9):1248-1258.   Published online September 30, 1989
To elucidate the characteristics of immunoregulatory system of children with chronic active hepatitis B and hepatitis B vaccine inoculated infant, the authors examined T cell subsets of the peripheral blood in 16 children with asymptomatic HBsAg carriers, 19 children with chronic hepatitis B (11 chronic persistent hepatitis (CPH) and 8 chronic active hepatitis (CAH) and 21 hepatitis B vaccine inoculated infants as well as...
A Case of Child Desquamative Interstitial Pneumonia.
Woo Taek Kim, Hyoung Doo Lee, Yung Tak Lim, Hee Joo Jeon, Hee Joo Park, Chan Yung Kim
Clin Exp Pediatr. 1989;32(1):92-100.   Published online January 31, 1989
Desquamative interstitial pneumonia (DIP) is a variant of idiopathic interstitial pneumonias, but characteristicalIy has massive desquamation and proliferation of alveolar cells into the distal air space with minimal fibrosis of the alveolar wall. DIP seems to have better response to corticosteroid and benign prognosis than idiopathic interstitial pneumonia. We experienced one case of 6-year old girl who showed typical picture of DIF on lung...
A Case of Addison's Disease.
In Hoon Lee, H. D. Lee, Hee Ju Jeon, Chan Yung Kim
Clin Exp Pediatr. 1988;31(12):1689-1695.   Published online December 31, 1988
A 9-year-old girl with Addison’s disease without other endocrine disorder presented with a brief review of the literature. The patient was transferee! to our hospital because of darkish brown pigmentation of whole body and generalized weakness which had misunderstood cyanotic heart disease. On physical examination, she was poorly nourished and below 10 percentile in weight and height. Skin and mucous membrane were diffusely darkish brown,...
Clinical Evaluation of Children with Psychiatric Problems Among Pediatric Patients.
Woo Tae Kim, Chan Yung Kim
Clin Exp Pediatr. 1988;31(9):1183-1192.   Published online September 30, 1988
The author has analysed 1080 cases of Pediatric patients visited Pediatric or psychiatric depart- ment for behavioral, emotional, or Psychiatric problems, from July 1982 to June 1987. The patients were categorized into three groups to observe the distribution of age, sex and disease, and the relation of symptom and disease, 127 cases consulted to Psychiatric department, 356 cases visited Psychiatric department directly, and 597...
Thyriod Function Studies in Children with Nephrotic Syndrome.
In Hoon Lee, Chan Yung Kim
Clin Exp Pediatr. 1988;31(8):1037-1047.   Published online August 31, 1988
To evaluate the influence of nephrotic syndrome on the thyroid function test in children, serum T3, T4, free T4, TSH, TBG and rT3 were measured using radioimmunoassay in 14 clinically euthyroid children with nephrotic syndrome who were admitted to Department of Pediatrics, Pusan National University Hospital from July, 1986 to August, 1987. Control group was 15 children who visit our outpatient department for minor...
The Two Cases of Klippel-Trenaunay Weber Syndrome.
Man Chul Ha, In Hun Lee, Yong Tak Lim, Hi Joo Chun, Hi Ju Park, Chan Yung Kim
Clin Exp Pediatr. 1988;31(3):391-397.   Published online March 31, 1988
We experienced two cases of Klippel-Trenaunay-Weber Syndrome in 13 years old boy and 10 years old girl. They had shown large nevus flammeus, varicose veins, soft tissue and bong hypatrophy. In angrogam and venogram capillary and venous hemangioma were noted, but we could not find arteriovenous filstula. We report two cases of Klippel-Trenaunay-Weber Syndrome with review of literature.
Liver Function Test in Congestive Heart Failure in Children.
Chan Yung Kim, Man Chul Ha
Clin Exp Pediatr. 1988;31(1):48-57.   Published online January 31, 1988
Clinical study was carried out on 149 congestive heart failure(CHF) cases of 873 heart disease patients admitted to the Department of Pediatics, Pusan National University Hospital from January 1980 to June 1987 and performed various diagnostic evaluations, especially liver function tests. The results obtained were as follows. 1) The congenital (CHD) and acquired (AHD) cause of heart disease were each 75.9% and 19.0% and the rest,...
Two Cases of Congenital Asplenia.
Man Chul Ha, Young Tak Lim, Hi Joo Chun, Hi Ju Park, Chan Yung Kim
Clin Exp Pediatr. 1987;30(8):916-921.   Published online August 31, 1987
Congenital absence of spleen is often associated with malpositions and malformations of other organ system such as congenital heart disease partial situs inversus, symmetric lobulation of the liver and the lungs. This is a rare syndrome but has been reported in increasing frequency in recent years. The pure congenital asplenia is a very rare disease. We experienced two cases of congenital asplenia. One is...
A Case of Wilson's Disease.
Hee Joo Jeon, Yong Joon Kim, Hi Joo Park, Chan Yung Kim, Jong Woo Shin
Clin Exp Pediatr. 1987;30(2):201-206.   Published online February 28, 1987
Department of Pediatrics, College of Medicine, Pusan National University Wilson’s disease is due to excessive accumulation of copper in the liver, brain, kidneys and cornea caused by a defect in biliary excretion. The classic presentation of Wilson’s disease is the triad of neurologic abnormalities, Kayser- Fleischer ring and cirrhosis associated with low serum copper and ceruloplasmin levels. The case, 12-year-old boy, suffered from jaundice, abdominal...
A Case of Relapsing Polychondritis
Yong Joon Kim, Hee Joo Jeon, Bong Joon Chung, Hi Ju Park, Sang Kun Jun, Chan Yung Kim
Clin Exp Pediatr. 1986;29(12):1360-1365.   Published online December 31, 1986
Relapsing polychondritis is a rare disease characterized by recurring episodes of inflammation of the cartilagenous structures of the body. Commonly involved organs include the inner and external ear, nose, joints, eyes, tracheobronchial tree, and cardiovascular system. We experienced a case of relapsing polychondritis in a 4 year old boy with auricular chondritis, polyarthritis, nasal chondritis, laryngeal chondritis and episcleritis. The review of...
Clinical Study of Diseases in Adolescence.
Chan Yung Kim, Yung Tak Lim
Clin Exp Pediatr. 1986;29(11):1168-1178.   Published online November 30, 1986
A clinical study was performed on 7,534 cases of disease entity and course in adolescence who were admitted to various department including internal medicine, pediatrics in Pusan National University Hospital from January 1980 to December 1985.The results are as follows: 1) The age distribution was from 10 years to 20 years of age which was devided to early adolescence in 21.2%,...
Case Report
A Case of Takayasu's Arteritis.
Bong Joon Chung, Man Cheol Ha, Yong Joon Kim, Chan Yung Kim
Clin Exp Pediatr. 1986;29(9):1007-1013.   Published online September 30, 1986
Takayasu’s arteritis is an arteritis of undetermined etiology which affects the aorta, the proximal portions of its major branches and pulmonary arteries. This 6 4/12-year-old female patient was developed hypertension and convulsion during" admission. At first we suspect rheumatic heart disease because of carditis, arthralgia, elevation of ESR, and presence of CRP and ASLO. But hypertension and congestive heart...
A Case of Cryptococcosis with Advanced Pulmonary Tuberculosis.
Hi Ju Park, Yong Joon Kim, Sang Kun Jung, Chan Yung Kim
Clin Exp Pediatr. 1986;29(1):95-100.   Published online January 31, 1986
This is a case of cryptococcosis accompanied by pulmonary tuberculosis and malnutrition. The 11-year-old female patient was admitted to our hospital because of dyspnea, ascites and oliguria. Cervical lymph node biopsy and chest X-ray were checked, which were revealed tuberculous lesions. She was treated with amphotericin-B for 10 weeks, but didn*t complete remission at present.
A Case of Spondylothoracic Dysplasia.
Jong Sic Joo, Bong Joon Chung, Yong Sub Kim, Kyung Hye Park, Chan Yung Kim
Clin Exp Pediatr. 1985;28(12):1221-1224.   Published online December 31, 1985
The author experienced a case of spondylothoracic dysplasia from 4 month old female-patient who had congenital anomalies on vertebrae & thorax. She was born with normal weight and full term, but she looked bizarre because of shortened trunk & neck, marked protuberant abdomen, prominent lumbar lordosis. On admission, she had growth retardation for having upper respiratory tract infection and feeding...
Original Article
Clinical Analysis of the Neck Mass in Childhood.
Jong Sic Joo, Chan Yung Kim
Clin Exp Pediatr. 1985;28(10):1007-1016.   Published online October 31, 1985
For evaluation of clinical characteristics, 228 cases of neck mass in childhood were reviewed, which were surgically removed and pathologically diagnosed during the period from January 1973 to August 1984 at the pediatric department of Pusan National University Hospital. The results are summarized as follows: 1)Histologically the most common lesion was nonspecific lymphadenitis (31.6%) and next was tuberculous lymphadenitis(17.1%). The congenital...
The Evolution of Serum Alpha-Fetoprotein Levels in the Newborn and Infants.
Gu Seok Jung, Chan Yung Kim
Clin Exp Pediatr. 1985;28(6):538-544.   Published online June 30, 1985
The author observed serum alpha-fetoprotein concentration in 112 cases of healthy, fullterm newborns and infants from March 1984 to September 1984. Among them, 9 cases were cord bloods of healthy, full-term newborns who were delivered at Pusan St. Benedict Hospital, the others were healthy infants under the age of 36 months who visited well-baby-clinic of Pusan St. Benedict Hospital. The...
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