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Original Article
Clinical Studies on Febrile Convulsion in Children.
Kang Ho Kim, In Kwyu Park, Young Bong Park, Jin Heon Kim, Chang Soo Ra
Clin Exp Pediatr. 1987;30(3):297-304.   Published online March 31, 1987
We have analyzed the clinical and laboratory findings of 204 patients with febrile convulsion, who were admitted to the Department of Pediatrics, Chosun University Hospital from Jan. 1976 to Dec. 1985. The results obtained were as follows: 1) In sex distribution, the boys(65.6%) outnumbered the girls(34.4%) and the ratio was 1.9:1. 2) 78.9% of the patients with febrile convulsion were from 6 months to under 4 years...
Case Report
A Case of Apert's Syndrome.
In Kwyu Park, Kang Ho Kim, Yeong Bong Park, Jin Heon Kim, Chang Soo Ra
Clin Exp Pediatr. 1986;29(9):1002-1006.   Published online September 30, 1986
Apert’s syndrome is an uncommon, congenital disturbance in the growth of bone and soft tissue affecting principally the head, the hand and feet. So there is skull malformation, most often acrocephaly, associated with symmetrical malformation of both hand and feet. This syndrome was first described by Apert in 1906. since that time, over 200 cases have been reported in the...
Original Article
Clinical Study of Acute Glomerulonephritis in Children.
Kyeong Rae Moon, Choon Ho Park, Sang Kie Kim, Jin Heon Kim, Chang Soo Ra
Clin Exp Pediatr. 1986;29(2):178-185.   Published online February 28, 1986
From January 1979 to June 1984, 96 cases of acute glomerulonephritis were clinically investigated at the Department of Pediatrics, Chosun University Hospital, and following results were obtained: 1) Male to female ratio was 1.7 : 1, and the age incidence was highest in children from 7 to 9 years (35.4%), with a seasonal peak in Autumn and Winter (66.8%). 2) The most common...
A Study on Calcium Metabolism in Newborn Infants.
Jin Heon Kim, Chang Soo Ra
Clin Exp Pediatr. 1985;28(10):967-976.   Published online October 31, 1985
A thorough understanding of calcium homeostasis and metabolism in newborn infants is necessary in the evaluation of any newborn infant with hypocalcemia. Author studied the levels of urinary calcium and phosphorus during the 48 hours after birth, and also studied before and after feeding during the 24 hours after birth in 19 normal term infants. And serum calcium, phosphorus, parathormone,...
Case Report
A Case of Peutz-Jeghers Syndrome.
Sang Kie Kim, Choon Ho Park, Jin Heon Kim, Keun Chul Myung, Chang Soo Ra
Clin Exp Pediatr. 1985;28(6):622-626.   Published online June 30, 1985
Peutz-Jeghers syndrome, also known as intestinal polyposis II, is a familial condition characterized by the triad of (1) mucocutaneous pigmentation, (2) benign polyps occuring in any part of the intestinal tract but mainly in the jejunum, and (3) autosomal dominant inheritance. This syndrome was first reported by Peutz in 1929. Following reemphasis by Jegers in 1949, it became a definite...
Adrenaogenital Syndrome with Congenital Adrenal Hyperplasia.
Kyeong Rae Moon, Yeong Bong Park, Sang Gi Kim, Jin Heon Kim, Chang Soo Ra, Jae Hong Seo, Ho Won Hwang
Clin Exp Pediatr. 1985;28(1):78-84.   Published online January 31, 1985
Adrenogenital syndrome is caused by a defect in biosynthesis of adrenal corticoids as a result of deficiency in one of the essential enzymes, most commonly 21-hydroxylase. About 50% of 21-hydroxylase deficiency have salt losing type as a result of aldosterone deficiency. We have experienced a casa of adrenogenital syndrome associated with congenital adrenal hyperplasia (salt losing form) in a 3...
A Case of Histiocytosis X(Hand-Schuller-Christian Syndrome).
Yeong Bong Park, Jin Heon Kim, Jong Myeon Hong, Chang Soo Ra
Clin Exp Pediatr. 1983;26(12):1209-1214.   Published online December 31, 1983
A case of histiocytosis X (Hand-Schuller-Christian syndrome) in a 3 year old girl is presented. The patients has the triad of exophthalmos, diabetes insipidus and skeletal lesions, plus hepatomegaly, wide spread pulmonary infiltration and growth retardation. The patient was treated with chlorambucil, prednisone, radiation therapy and chlorpropamide therapy for diabetes insipidus with good response. Similar cases reported in literature are briefly...
Nephrogenic Diabetes Insipidus occurred in 2 Brother.
Jin Heon Kim, Cheol Won Park, Bong Soo Lee, Chang Soo Ra
Clin Exp Pediatr. 1983;26(9):916-921.   Published online September 30, 1983
Nephrogenic diabetes insipidus is a congenital hereditary disorders in which the kidney do not respond to vasopressin, and the disease occurs principally in males and is probably inherited by Xlinked recessive mode. We experienced two cases of nephrogenic diabetes insipidus occurred in brothers. The clinical manifestations were extreme thirst and frequent urination of large volume of dilute urine, approximately 5,500ml per day with specific gravity...
A Case of Myelofibrosis.
Ho Seong Yoo, Jin Heon Kim, Keun Chul Myung, Chang Soo Ra
Clin Exp Pediatr. 1983;26(8):829-834.   Published online August 31, 1983
Myelofibrosis is characterized by fibrosis of bone marrow, leukoerythrobla stotic anemia and extramedullary hematopoesis with varying degree of hepatosplenomegaly. Idiopathic myelofibrosis is primarily a disease of the adult and is rare in the pediatric age group. We experienced a case of idiopathic myelofibrosis in a 2 year 5 month old male who showed severe anemia with abnormal forms of red blood cell (teardrops, ovalocytes),...
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