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Original Article
Clinical Observation of Rheumatic Fever and Rheumatic Heart Disease in Children.
Soon Don Hong, Sung Ho Cha, Chang Il Ahn
Clin Exp Pediatr. 1986;29(6):596-603.   Published online June 30, 1986
Acute rheumatic fever is an inflammatory disease of the heart, joint, central nervous system, and subcutaneous tissues which developes after a nasopharyngeal infection by group A beta-hemolytic Streptococci. Rheumatic fever is especially important to pediatrician because of the most acquired heart disease which usually ensues. To analyze the 101 cases of rheumatic fever and rheumatic heart disease in pediatric department of...
A Case Report of Ventricular Septal Defect and Aortic Valve Insufficiency Occurred in Siblings.
K H Kim, S S Kim, J H Sul, S K Lee, D S Chin
Clin Exp Pediatr. 1985;28(4):386-389.   Published online April 30, 1985
The occurrence of congenital heart disease can be explained by genetic or environmental aspects. But these factors act separately only in about 10% and most of all, which reaches up to 90%, are inherited by the pattern of multifactorial inheritance, in which there is an underlying genetic predisition, usually produced by the small effects of many genes interacting with an...
Heart Disease Screening for Primary School Children.
Chang Yee Hong, In Sil Lee, Hee Ju Kim, Jung Hwan Choi, Hae Il Cheong, Jung Yun Choi, Yong Soo Yun
Clin Exp Pediatr. 1985;28(3):258-262.   Published online March 31, 1985
A heart disease screening program was performed on 15,685 primary school children in Seoul City from the first to sixth grade to estimate the prevalence of heart diseases. Among the 15,685 children examined, 45 were confirmed to have heart disease (2.9/1,000) Out of the 45 children, 38 had congenital heart disease(2.4/1,000) and 7 had rheumatic heart disease(0.4/1,000) and the ratio...
Case Report
Fatal and Neonatal Arrhythmia: 3 cases.
Seon Ock Khang, Eui Soo Park, Heung Jae Lee, Keun Soo Lee
Clin Exp Pediatr. 1984;27(10):1000-1005.   Published online October 31, 1984
Authors experienced three cases of arrhythmia which were assumed to be present from their fetal lives. One of cases was congenital complete heart block with Adams-Stokes attacks who had the history of severe fetal bradycardia. The other two cases had benign supraventricular ectopic beats with spontaneous recovery within two months of age. Fetal tachycardia was observed in one case with multifocal...
Original Article
Echocardiographic Evaluation of Pulmonary Arterial Hypertension in Pediatric Congenital Heart disease.
Myoung Sung Moon, In Hee Park, Heung Jae Lee, Hahng Lee, Keun Soo Lee
Clin Exp Pediatr. 1984;27(10):971-981.   Published online October 31, 1984
To assess the validity of Echocardiographic criteria for pulmonary arterial hypertension we studied pulmonary valve motion in 75 congenital heart disease children. 75 patients were divided into two groups, A and B. The group A consisted of 39 patients who had normal pulmonary arterial pressure, group B consisted of 36 patients who had pulmonary arterial hypertension(pulmmonary artery mean pressure more...
Case Report
Two Cases of Complete Atrioventricular Block Associated with Adams-Stokes Attack in Childen.
Y K Suh, H D Cha, S H Kim, T C Kwon, C M Kang
Clin Exp Pediatr. 1984;27(9):918-923.   Published online September 30, 1984
Authora experienced two cases of complete Atrioventricular block with Adams-Stokes attack in a 14 year old boy and a 5 year old girl who were admitted to the Pediatric Department of Dong-San hospital, Keimyung University. Both cases had typical syncopal attack as a first time and complete Atrioventricular block on electrocardiogram. There was.no specific past history and no associated congenital heart...
Original Article
A Clinical Observation on Isolated Ventricular Septal Defect In Children.
Chang Ho Lee, Kwang Do Lee, Sang Bum Lee, Ja Hoon Koo
Clin Exp Pediatr. 1984;27(7):702-710.   Published online July 31, 1984
A clinical study was done an 39 cases of isolated VSD who had been admitted to the Pediatric Department of Kyungpook National University Hospital, and and confirmed by cardiac catheterization during the period from January 1975 to May 1983. The results were as follows; Out of 77 cases of congenital heart disease underwent cardiac catheterization, 39 cases were isolated VSD,...
Congenital Heart Disease in Neonatal Period and Infancy .
Jung Yun Choi, Hey Sun Lee
Clin Exp Pediatr. 1984;27(6):570-582.   Published online June 30, 1984
From July 1980 to June 1983, total 468 cases of infants of congenital heart disease were studied, who needed intensive care in infancy at Seoul National University Hospital. 1)Among 468 cases, 285 cases were diagnosed by cardiac catheterization or cardiac surgery and the other 183 cases by only clinical base. 2)Relative frequencies of these individual anomalies were in order of...
Case Report
Two Cases of Anomalous Origin of the Right Pulmonary artery from the Ascending Aorta.
Kyu Gap Hwang, Gu Soo Kim, Jung Yun Choi, Yong Soo Yun, Chang Yee Hong
Clin Exp Pediatr. 1984;27(5):501-505.   Published online May 31, 1984
Anomalous origin of one pulmonary artery from the ascending aorta is a rare congenital malformation. It happens as the result of abnormal development of the 6th aortic arch. Anomalous origin of right pulmnary artery is more frequent than left. It is frequently associated with P.D.A., V.S.D. and T.O.F. In this malformation, congestive heart failure develops in early life and once the...
Original Article
A Clinical Study of Cor Triatriatriatum.
Jae Ho Lee, Il Suck Chang, Nam Su Kim, Yong Soo Yoon, Chang Yee Hong
Clin Exp Pediatr. 1983;26(11):1070-1080.   Published online November 30, 1983
Cor triatriatum is a rare congenital cardiac anomaly in which the left atrium is divided into two chambers by an abnormal fibro-muscular septum with, a small opening or not, product pulmonary venous obstruction and pulmonary hypertension. Three cases of cor triatriatum were observed at the Dept, of Pediatrics, Seoul National University. Each patient had no specific problem during early infancy, and presented...
Case Report
A Case of Conjoined Twins.
Kyu Gap Hwang, Myung Hyun Lee, Choung Ku Yun
Clin Exp Pediatr. 1983;26(7):696-701.   Published online July 31, 1983
Conjoined twins are rare malformation. It appears with the frequency of 1 in 50,000. Conjoined twins offer excellent model systems for problems concerning organizing phenomenon, symmetry of hcdy plane and teratogenesis. In our hospital, we experienced a case of craniopagus. They were admitted to our hospital for 6 months. At 6month of age, twin 2 died of congestive heart failure in spite of treatment. We...
A Case of Hypereosinophilic Syndrome.
Chang Moo Lee, Chull Kwon Chung, Soon Ok Byun, Ji Sub Oh
Clin Exp Pediatr. 1983;26(2):193-197.   Published online February 28, 1983
We experienced a case of Hypereosinophilic syndrome with congestive heart failure in 15 month old girl. The clinical, hematologic and E.C.G. findings were compatible with hype- reosinophilic syndrome. She was treated with oxygen, digoxine, antibiotics and mebendazole. But on 8th day of admission she suddenly died. A brief review of the related literature was made on this subject.
Original Article
Cardiac Arrhythmia in Infants and Children.
Jun Hee Kang
Clin Exp Pediatr. 1982;25(3):234-240.   Published online March 31, 1982
Cardiac arrhythmia which was observed during 5 years and 10 months from September 1975 to June 1981 on 11, 273 ECG records of the pediatric patients were analysed. Simple sinus arrhythmia and bundle branch blocks were excluded from this study. 602 cases of arrhythmia were seen among the 11,273 cases(5.3%). The types of arrhythmia in the order of frequency are:...
Case Report
There cases of Hereditary Anhidrotic Ectodermal Dysplasia.
Seung Woo Moon, Seung Koo Park, Jung Ju Kim, Dong Hak Shin, Sang Suk Lee
Clin Exp Pediatr. 1982;25(1):80-88.   Published online January 31, 1982
Hereditary anhidrotic ectodermal dysplasia is a rare hereditary condition in which certain structures derived from the ectoderm are undeveloped or underdeveloped, although, on a rarity, mesodermal or endodermal derivatives may be associated. Recently, we enperienced 3-cases of anhidrotic ectodermal dysplasia in 3 months male infant and in brothers aged 4(1/2) months and 22 months. They had abscence of sweating, hypotrichosis...
A Case of Left Ventricular-Right Atrial Shunt.
Myung Chul Kang, Hyun Kyung Cho, Kyong Su Lee, Du Bong Lee, Kyung Sub Shinn, Hong Kyun Lee
Clin Exp Pediatr. 1982;25(1):66-71.   Published online January 31, 1982
Left ventricular-right atrial shunt is a relatively uncommon defect, which permits as communication between the left ventricle and right atrium. This paper is fifth case report in our country. This patient was noted to have congenital heart disease in two years old. The pathology of this lesion was classified into four types by Perry. The type C is compatible with...
Original Article
The Heart in Acute Glomerulonephritis: An Echocardiographic Study.
Eun Hee Choi, In Hyun Cho, Sun Ja Lee, Dong Hyuck Keum
Clin Exp Pediatr. 1981;24(7):659-665.   Published online July 15, 1981
Patients with acute glomerulonephritis often are seen with signs suggesting heart failure. Whether these signs are due to fluid overload secondary to kidney damage only, or whether there is associated myocardial damage has not been elucidated. Twenty-two children with acute glomerulonephritis were studied by echocardiography during edematous phase of disease. Left ventricular function was normal in all childrem. The most...
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