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Case Report
A Case of Sturge-Weber Syndrome.
Soo Young Kim, Hyang Sook Kim, Myung Sook Kim, So Young Park, Dong Hak Shin
Clin Exp Pediatr. 1981;24(11):1111-1115.   Published online November 15, 1981
Recently, we experienced a case of Sturge-Weber Syndrome in a 9 month old female. The diagnosis was established by typical clinical features of Sturge-Weber Syndrome in eluding facial portwine nevus, convulsion, left hemiparesis, glaucoma and typical calcification & brain atrophy as seen on on the brain CAT. Plain radiolographys of the skull revealed no evidence of calcification, while the brain...
A Case of Marfan's Syndrome.
Ki Hyun Yoon, Jung Suh Suh, Son Sang Suh, Jong Woo Shin
Clin Exp Pediatr. 1981;24(11):1106-1110.   Published online November 15, 1981
We have experinced a case of Marfan’s syndrome'in 27 months old female children. Marfan's syndrome is characterized by skeletal, ocular and cardiovascular abnormalities. Diagnosis was established by clinical characteristics with radiologic and laboratory findings. Pertiment literatures on Marfan’s syndrome also reviewed briefly.
A Case of Cushingoid syndrome Associated with Mediastinal Lipomatosis, Aseptic Necrosis of Hip Joint and Growth Retardation.
Chang Woo Koh, Hyung Jin Choi, Chang Hwi Kim, Sang Man Shin, Sang Jhoo Lee
Clin Exp Pediatr. 1981;24(10):973-981.   Published online October 15, 1981
The 15 year-old female patient was admitted with the complaints of moon face, obesity and short stature. She has received steroid therapy since 11 years ago at home to control joint pain due to rheumatoid arthritis. The diagnosis was confirmed by history of long-term steroid therapy, characteristic clinical features, biochemical studies and radiological studies. In radiological studies, superior mediastinal widening,...
A Case of D1-Trisomy Syndrome.
Soon Hee Choi, Seung Joo Lee, Keun Lee
Clin Exp Pediatr. 1981;24(10):968-972.   Published online October 15, 1981
One cases of D1-Trisomy Syndrome which was confirmed by chromosome study at Ewha Womans University Hospital is presented. The premature female infant was delivered spontaneously at 36 1/2 weeks of gestation at Ewha Womans University. The family and antenatal history were not remarkable except ingestion of some kinds of antibiotics and anti-inflammatory drugs during the first trimester. On physical examination...
Mucocutaneous Lymph Node Syndrome: Report of one case complicated by gallbladder hydrops and diagnosed by ultrasound.
Chul Ho Lee, Sung Won Park, Chang Soo Han, Soon Jai Lee, Yeun Ki Kim
Clin Exp Pediatr. 1981;24(9):877-881.   Published online September 15, 1981
A female patient with mucocutaneous lymph node syndrome is presented. During the course of her illness, she developed acute abdominal pain secondary to hydrops of gallbladder. The diagnosis was facilltated by ultrasound. We managed her conventionally without surgical intervention. It is interesting that the age of patients complicated by gallbladder hydrops is high compared with the age frequency of MCLS....
Original Article
Cluster of Guillain-Barre Syndrome.
Young Mo Sohn, Sung Sik Lee, Kwan Sub Chung, Ki Sub Chung, Seung Kyu Lee, Pyung Kil Kim, Kir Young Kim, Duk Jin Yun, Kyoung Ja Cho
Clin Exp Pediatr. 1981;24(9):820-825.   Published online September 15, 1981
Of 7 cases of Guillain-Barre syndrome reviewed, which was admitted to the Department of Pediatrics Yonsei University, College of Medicine during 3 months period from July through September 1980, serologic surveys for an infectious agent were found to be without demonstrable causes such as cytomegalovirus and measles virus. We reviewed 87 acses of Guillain-Barre syndrome, which was admitted to our...
Case Report
A Case of Beckwith Syndrome.
Kyung Tae Kim, Dae Sik Hong, Byung Do Nam, Kew Taek Kim
Clin Exp Pediatr. 1981;24(7):696-698.   Published online July 15, 1981
We experienced one case of Beckwith syndrome. This one day aged male neonate manifested macroglossia, umbilical hernia, visceromegaly, hypoglycemia, gigantism and polycythemia. A brief review of related literature is also presented.
Original Article
Diagnostic Value of Serum Immunoglobulins in Glomerulonephritis.
Pyung Kil Kim, Kyo Sun Kim, Chul Lee, Nan Ae Kim, Jae Seung Lee
Clin Exp Pediatr. 1981;24(7):652-658.   Published online July 15, 1981
Serum immunoglobulin concenatrations were measured in 156 patients with various types of glomerulonephritis such as acute poststreptococcal glomerulonephritis, minimal lesion nephrotic syndrome and Henoch-Sch?lein purpura nephritis. 1) Serum IgG level was above normal mean in acute poststreptococcal glomerulonephritis, and normal range in Henoch-Scholein purpura nephritis. Serum IgG concentrations were significantly reduced in minimal lesion nephrotic syndrome. 2) Serum IgA concentrations...
Clinical Study on Idiopathic Nephrotic Syndromein Children.
Haeng Mi Kim, Chang Ho Lee, Ja Hoon Koo, Doo Hong Ahn
Clin Exp Pediatr. 1981;24(6):549-558.   Published online June 15, 1981
A clinical observation was done on 38 children with idiopathic nephrotic syndrome, who had been admitted to our pediatric department during past 3 years period, from January 1978 to September 1980. The following results were obtained: At the beginning of illness, 42% were in the age group of 3~7year, and male to female ratio was approximately 3:1 of male preponderance....
Form Stability Test on Gastric Aspirate and Respiratory Distress Syndrome in Newborn Baby.
Byung Do Nam
Clin Exp Pediatr. 1981;24(5):437-444.   Published online May 15, 1981
Form stability test on gastric aspirate was performed on 102 cases of newborn within 30 minutes afterbirth, who were admitted to Special Care Unit of St. Benedict Hospital from Sep. 1977 to Aug. 1979, and following results were obtained. 1) There was no differnce between amniotic fluid and gastric aspirate in control group. 2) In all newborn infants with positive...
Case Report
Recurrent Guillain-Barr'e Syndrome.
Kyo Sun Kim, Jae Song Kim, Pyung Kil Kim
Clin Exp Pediatr. 1981;24(4):367-450.   Published online April 15, 1981
This paper presents a case of^recurrent Guillain-Barre syndrome in a 13 year-old boy. Recu-rrent rate is variable but almost all of the authors expressed it was very rare and some of them recurred more than two times and and its interval also variable from few months to 17 years. In our case, he developed a typical ascending, symmetric motor paralysis...
Hepatorenal Syndrome.
Kyo Sun Kim, Young Mo Sohn, Jung Soo Kim, Jae Seung Lee, Pyung Kil Kim, Tae Jung Kwon, In Jun Choi
Clin Exp Pediatr. 1981;24(3):257-270.   Published online March 15, 1981
Hepatorenal syndrome is generally urged, at least until specific interrelationships between the two organs are confirmed by experimental and clinical data. Case I was a 11 year old boy, who had been suffered from acute fulminant viral hepatitis, which had developed acute hepatic necrosis associated with acute renal failure. Cass H was a 10 year old girl, who was performed corrective...
A case of Congenital Syphilitic Nephrotic Syndrome.
H S Kim, S K Park, D H Shin
Clin Exp Pediatr. 1981;24(1):94-99.   Published online January 15, 1981
We have experienced a case of congenital syphilitic nephrotic syndrome in a 4 months old boy, who was admitted to presbyterian hospital, Daegu, Korea. He was sucessfully treated with penicillin of 2 weeks duration. We made brief review of the related literatures.
A Case of Cushing's Syndrome Associatied with Hypertensive Encephalopathy.
Choong Rae Kim, In Soon Park, Do Seung Lee, Jae Sun Park, Kee Ryo Chang, Soon Yong Lee
Clin Exp Pediatr. 1981;24(1):80-84.   Published online January 15, 1981
A 8-yrs-old boy was admitted because of convulsion and coma. The diagnosis of Cushing's syndrome(key word) associated with hypertensive encephalopathy(key word) due to right adrenocortical carcinoma(key word) was made by clinical features, biochemical studies, radiological studies and pathological examination. The tumor was successfully resected by right adrenalectomy. But 22 months later after operation, he died of dyspnea and heart failure....
Original Article
Effect of the Glucocorticoids on the Vertebral Bone Density in Children with the Nephrotic Syndrome
Jong Young Kim, Yong Hoon Park
Clin Exp Pediatr. 1955;38(7):946-954.
Purpose : This study was conducted to evaluate that long term glucocorticoid treatment in children with the nephrotic syndrome can produce a significant loss of bone mass by measuring of bone mineral density(BMD) Methods : We measured BMD at lumbar vertebra(L2-L4) using dual enegy X-ray absorptiom-etry in 36 patients with the nephrotic syndrome who were administered prednisolone over 6 months and...
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