• Search
  • Advanced Search

Search

  • HOME
  • Search
Original Article
A Study on Serum Growth Hormone in DM of Childhood.
Duk Hi Kim
Clin Exp Pediatr. 1987;30(2):175-180.   Published online February 28, 1987
The human growth hormone (hGH) levels were evaluated in 13 diabetes mellitus, 11 patients were insulin dependent diabetes (ages 2 yr 10 mo to 13 yr 14 mo), 2 patients were noninsulin dependent diabetes (age 12 yr & 12 yr 5 mo). No difference in hGH level was observed in relation to duration of diabetes. The hGH responses to glucagon 1 mg injection in...
Case Report
Hodgkin’s Disease in Children
Soo Jong Hong, Hyo Seop Ahn, Chang Yee Hong
Clin Exp Pediatr. 1986;29(12):1352-1359.   Published online December 31, 1986
Twenty one cases of Hodgkin’s disease under 15 years of age who were admitted to Dept, of Ped. of Seoul National University Hospital from Jan. 1976 to Dec. 1985 were reviewed and analysed. One hundred and five cases of non-Hodgkin’s lymphoma were seen during the same period. 1) The ratio of non-Hodgkin’s lymphoma to Hodgkin's disease was 5:1. 2) The age ranged from 18/12 years...
A Case of Potter Syndrome Type I.
Jong Cheol Ryu, Jae Kwang Hong, Jun Taek Park, Jung Sik Min, Chang Jee Choi, Je Geun Chi
Clin Exp Pediatr. 1986;29(10):1152-1156.   Published online October 31, 1986
We have experienced a case of Potter syndrome type I in a newborn infant who presented with severe respiratory distress soon after birth. The diagnosis was made with autopsy findings consisted of bilateral polycystic renal dysplasia, bilateral hypoplastic lung , facies renalis, fibrocystic change of liver, patent ductus arteriosus, patent foramen ovale, ureter and urinary bladder hypoplasia and calcaneovarus. Brief...
Original Article
Studies on Type A and Type B Acute Hepatitis in Children.
Moo Young Oh, Soon Ho Kim
Clin Exp Pediatr. 1986;29(7):740-747.   Published online July 31, 1986
The author investigated incidence, age and sex distribution and some liver function tests in 128 cases of type A acute hepatitis and in 62 cases of type B acute hepatitis of children who were admitted to the pediatric ward of Busan In Je Medical college Hospital from January, 1982 to August, 1984. Diagnosis was established clinically and serologically in all patients....
Twelves Cases of Thyroid Carcinoma in Children.
Yong Woo Choi, Myung Ho Cho, O Kyung Lee, Myung Ho Lee
Clin Exp Pediatr. 1986;29(6):661-667.   Published online June 30, 1986
We obtained following results by analysis of 12 cases of thyroid carcinoma in patient under 15 years of age who were admitted to Presbyterian Medical Center, Chon-ju from January 1975 to December 1984. 1) The ratio between male and female patients was 1 : 3. Patients over 12 years of age totalled 7 cases(58.3%). The youngest patient was 5 years and...
Case Report
A Case of Osteogenesis Imperfecta.
Kwang Wook An, Chull Zoo Jung, Hyo Seop Joo, Seung Woo Moon
Clin Exp Pediatr. 1986;29(1):84-87.   Published online January 31, 1986
Osteogenesis imperfecta is an inherited disorders of connective tissue that affects the skeleton, ligament, sclera, and dentin. Characterized clinical manifestation are multiplefracture, blue sclera, deafness, joint laxity, thin skin, and odontogenesis imperfecta. We experienced acase of osteogenesis imperfecta in a one day old male newborn who chiefly complain respiratory distress, triangular shaped head and fracture and deformity of lower extremity....
4 Cases of Progressive Muscular Dystrophy.
Jung Hee Kim, Dong Wook Kim, Dae Deok Ahn, Jung Kwon Lee, Yoon Ja Kim
Clin Exp Pediatr. 1985;28(12):1225-1230.   Published online December 31, 1985
Progressive muscular dystropy is a genetically determined disorder characterized by-progressive weakness and wasting of skeletal muscles. The etiology of muscular dystropy is unknown, and no form of phamacological treatment is considered effective. The authors report 4 cases of P.M.D., of which 2 cases occured in a family and 2 cases were developed sporadically. They were diagnosed by clinical findings, serum,...
Original Article
A survey of chromosome studies in 466 cases.
In Sung Lee, Cheol seung Son, Ki Bok Kim
Clin Exp Pediatr. 1985;28(2):160-168.   Published online February 28, 1985
The results of chromosomal studies performed at the Dept, of Pediatrics, Kwangju Christian Hospital from March 1974 to May 1984 were analyzed as to the clinical categories. Out of total 514 cases subjected to chromosomal studies, karyotype patterns were obtained in 466 cases, the success rate reaching 91%. Fifty two percent of all cases subjected to karyotype analysis were under...
Case Report
A Case of Congentital Leukemia.
Joon Sik Kim, Chang Ik Lee, Dong Hak Shin
Clin Exp Pediatr. 1984;27(8):802-807.   Published online August 31, 1984
Congenital leukemia is rare disease and several cases were reported in this country. We experienced a case of congenital leukemia(myelomonocytic type) in a 27 days old female. She was admitted due to marked abdominal distension, vomiting and generalized petechia. The diagnosis was established by clinical features as well as peripheral blood and bone marrow studies. We report this case with...
A Case of Glycogen Storage Disease Type IIa.
Dong Hyung Choo, Dong Kyoon Kim, Hyung Ro Moon, Choong Kon Kim
Clin Exp Pediatr. 1984;27(6):621-627.   Published online June 30, 1984
Glycogen storage disease type Ha(GSD la), also known as generalized glycogenosis, cardiomegalic glycogenosis, and Pompe disease, is a very rare form of glycogenosis. The authors reported a case of GSD J a in an eight months old girl who presented with respiratory problems, marked hypotonia, cardiomegaly, and macroglossia. The diagnosis was made on clinical grounds including pathologic findings of muscle...
A Case of Osteogenesis Imperfecta Type II.
Chang Ick Lee, Young Ai Kim, Jung Joo Kim, Dong Hak Shin
Clin Exp Pediatr. 1984;27(1):93-97.   Published online January 31, 1984
Osteogenesis, imperfecta is an inherited disorder of connective tissue characterized by multiple fractures, blue sclerae, progressive deafness, loose jointedness, and skin. We experienced a case of Type I osteogenesis imperfecta in a 2 months old male infant who visited our hospital with chief complaints of generalized growth retardation, blue sclera and frequent fractures and deformities of limbs. With typical manifestation...
Pulmonary Sequestration intralobar Type.
San Ho Kim, Jong Bum Kim, Dae Yeol Lee, Jong Jin Won
Clin Exp Pediatr. 1983;26(9):899-904.   Published online September 30, 1983
Pulmonaary sequestration is a relatively uncommon anomaly that usually requires arteriography for definitive diagnosis. We recently experienced a case in which the diagnosis of intraloar pulmonary sequestration was confirmed by aortogram & surgery. The patient was 9 years old female with the chief complaint of coughing, fever, sweating, and myalgia. The sequestration was resected by lobectomy. The authors report a case of...
Original Article
Supracristal Ventricular Suptal Defect in Korean.
Hee Ju Kim, Son Moon Shin, Yong Soo Yoon, Chang Yee Hong, Yung Kyoon Lee
Clin Exp Pediatr. 1983;26(7):631-639.   Published online July 31, 1983
Supracristal ventricular septal defect has engendered an interest in recent years because of the racial difference in its incidence and the unusually high association of the aortic valve abnormalities. The relative incidence of supracristal ventricular septal defect was studied in Korean. During the period of eight years from January 1974 to December 1981, 119 cases(27.6%) of supracristal type were noted among 431 cases of...
Case Report
A Case Report of Ectopic Cords.
Sang Cheol Lee, Jae Gae Rue, Byung Do Nam, Jung Hee Lee
Clin Exp Pediatr. 1983;26(3):275-278.   Published online March 31, 1983
A case of thoracic ectopia cordis in a female newborn baby was presented. The patient manifested a pulsating mass protruding out of the midline of the thorax, split sternum, skin defect of a abdominal wall, and left ventricular diverticulum, and she had several extracardiac anomalies such as hepatomegely, absence of gall bladder and common bile duct, and blind ending of both...
Original Article
Clinical and Hematological Analysis on the 110 Cases of Childhood Leukemia.
Sang Choel Lee
Clin Exp Pediatr. 1982;25(12):1252-1260.   Published online December 31, 1982
The author reviewed the clinical and hematological findings of the 110 children diagnosed as leukemia at pediatric departments, Busan National University and St. Benedict’s Hospital, Busan, during a period of 8 years arid 8 months from January 1973 to August 1981. The results obtained were summarized as follows: 1. Of the 110 chil-dhood leukemias, acute lymphoblastic type was most frequent(60.9%), iollowed by acute myeloblastic...
HLA Type in Bronchial Asthma and Atopic Dermatitis.
Ji Yoon Chung, Myung Sook Kim, Jung Ju Kim, Dong Hak Shin
Clin Exp Pediatr. 1982;25(5):460-466.   Published online May 31, 1982
Since the histocompatibility was discovered, we have studied and determined many HLA types till the last workshop held in Los Angeles, USA, 1980. Nowadays we apply HLA types to organ transplantation, transfusion of blood, identification of paternity, study of ethnology and diagnosis of a specific disease. In the present study, 20 cases of bronchial asthma and 15 atopic dermatitis patients...
Case Report
A case of Finnish Type of Congenital Nephrotic Syndrome.
Jeong Sik Min, Yang Kook Shon, Soo Woong Lee, Suk Chul Kang, Yong Koo Park, Moon Ho Yang
Clin Exp Pediatr. 1982;25(2):175-182.   Published online February 28, 1982
The Finnish type of Congenital Nephrotic Syndrome is characterized by large placenta, early manifestation, growth and developmental delay and resistance to treatment. Authors experienced a case of characteristic Finnish type of Congenital Nephrotic Syndrome in a girl, who was admitted to the Pediatric Department of KHUH at 2 1/1 months of age because of generalized edema and abdominal distension and...
Original Article
A Case-Control Study on the Factors Influencing Neonatal Hyperbilirubinemia.
Kwang Ho Meng, Won Chul Lee, Kyung Tai Whang
Clin Exp Pediatr. 1982;25(2):136-140.   Published online February 28, 1982
Neonatal Hyperbilirubinemia is increasing in frequency and there have been suggestions that this may be due to some change in factors involved in delivery. In this study, among numerous hypothesized factors, maternal age, gestational age, birth weight, birth order, and methods of delivery were tested if there were statistical associations between these factors and occurance of neonatal hyperbilirubinemia. For the...
Case Report
A Case of Progressive Muscular Dystrophy.
Myung Sook Kim, Kyung Sook Choi, Jung Ju Kim, Dong Hak Shin, Sang Sook Lee
Clin Exp Pediatr. 1982;25(1):97-101.   Published online January 31, 1982
We want to report one case of Duchenne type muscular dystrophy in a female. This patient was seven years of age. Clinical symptoms first appeared at age 3 and progressed insiduously. The Gower's sign was positive. She had a borther who had similar clinical signs and symptoms. He died at age 12. An increased ratio of creatine and creatinine was...
Duchenne Type Muscular Dystrophy Occuring in 2 Brothers.
Bong Soo Lee, Jon Kerl Lee, Chang Soo Ra
Clin Exp Pediatr. 1981;24(3):271-274.   Published online March 15, 1981
We were experienced. Duchenne typs muscular dystrophy occuring in brothers of 13years and 18years old boy. In all cases, ssrum CPK levels were significantly increased and typical waddling gait and Gowers sign were noticed, the muscle biogsy findings were also compatible with progressive muscular dystrophy. We report with brief review of literatures.
TOPICS

Browse all articles >

ARTICLE CATEGORY

Browse all articles >

BROWSE ARTICLES
FOR CONTRIBUTORS
ABOUT
Editorial Office
Korean Pediatric Society
#1606 Seocho World Officetel, 19 Seoun-ro, Seocho-ku, Seoul 06732, Korea
Tel: +82-2-3473-7306    Fax: +82-2-3473-7307    E-mail: office@e-cep.org                

Clinical and Experimental Pediatrics is an open access journal. All articles are distributed under the terms of the Creative Commons Attribution NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/)

Copyright © 2026 by Korean Pediatric Society.      Developed in M2PI