1.Clinical Study of Diseases in Adolescence.
Journal of the Korean Pediatric Society 1986;29(11):8-18
No abstract available.
Adolescent*
;
Humans
2.A Clinical Observation on Failure to Thrive.
Journal of the Korean Pediatric Society 1987;30(3):259-265
No abstract available.
Failure to Thrive*
3.A Case of Addison's Disease.
In Hoon LEE ; Yung Tak LIM ; Hee Ju JEON ; Chan Yung KIM
Journal of the Korean Pediatric Society 1988;31(12):1689-1695
No abstract available.
Addison Disease*
4.Primary Hyperparathyroidism in Children
Han Sang CHO ; Sang Ook PARK ; Byung Mun LEE ; Yung Tak LIM ; Su Yung KIM
Journal of Korean Society of Endocrinology 1994;9(3):251-257
Primary hyperparathyroidism is a rare endocrine disease in children. It involves bone and joint, urinary tract, gastrointestinal tract and cardiovascular system. The main cause of these involvement is high level of PTH in serum, resulting in hypercalcemia.An 11 years old male patient who had complained of limping gait since last 18 months, showed typical laboratory and radiological findings of primary hyperparathyroidism. At the ultrasonography, computed tomography and radionuclide scanning, a well defined mass(10 X 15mm) was found on the posterior aspect of the right thyroid lobe. The mass was confirmed histologically as adenoma of parathyroid gland. The patient was successfully treated with subtotal parathyroidectomy and temporal administration of calcium and vitamin D.We report this case of primary hyperparathyroidism with brief review of the literatures.
Adenoma
;
Calcium
;
Cardiovascular System
;
Child
;
Endocrine System Diseases
;
Gait
;
Gastrointestinal Tract
;
Humans
;
Hyperparathyroidism, Primary
;
Joints
;
Male
;
Parathyroid Glands
;
Parathyroidectomy
;
Thyroid Gland
;
Ultrasonography
;
Urinary Tract
;
Vitamins
5.A Case of Child Desquamative Interstitial Pneumonia.
Yung Tak LIM ; Hee Joo JEON ; Hee Joo PARK ; Chan Yung KIM ; Woo Taek KIM ; Hyoung Doo LEE
Journal of the Korean Pediatric Society 1989;32(1):92-100
No abstract available.
Child*
;
Humans
;
Lung Diseases, Interstitial*
6.A Clinical Study on Chronic Hepatitis B in the Children.
Bon Su KOO ; Han Sang JO ; Yung Tak LIM ; Hee Ju PARK
Journal of the Korean Pediatric Society 1994;37(6):767-775
The author observed clinical study and response of -interferon treatment of 43 cases of chronic hepatitis who were admitted to Department of Pediatrics Pusan National University College of Medicine during the period of 4 year 6 months from Jenuary, 1988 to Jun, 1992. The results were as follows: 1) Of 43 patients with chronic hepatitis, CPH was 17 cases (39.5%) and CAH was 26 cases (60.5%). 2) Of 43 patients, chronic hepatitis caused by HBV was 37 cases (86.0%) 2 cases were by Wilson's disease, 1 case was by glycogen storage disease and in the 3 cases, the cause was undetermined and CPH by HBV and CAH were 14 cases (82.4%), 23 cases (88.5%) respectively. 3) A peak frequency (46.5%) of chronic hepatitis occurred between 6 to age and male predominated in a propotion of 3.5:1. 4) On the clinical manifestation, jaundice and hepatomegaly was higher frequency on CAH than on CPH. 5) On the laboratory findings, CAH had higher serum ALT and direct bilirubin level than CPH. 6) On effect of -interferon treatment for patients of CAH, serum ALT and AST levels normalized in 81.8% of patients, negative conversion of HBeAg was 38.5%, Anti-HBe serocoversion was 7.7%, negative conversion of HBsAg was 7.7% and the clearnce of HBV-DNA from seum showed 60.0%. 7) The HBeAg seroconversion (28.6%) on children of HBsAg(+) mother showed lower reponse than HBeAg seroconversion (50.0%) of HBsAg(-) mother after -interferon treatment for patients of CAH.
Bilirubin
;
Busan
;
Child*
;
Glycogen Storage Disease
;
Hepatitis B e Antigens
;
Hepatitis B Surface Antigens
;
Hepatitis B, Chronic*
;
Hepatitis, Chronic*
;
Hepatolenticular Degeneration
;
Hepatomegaly
;
Humans
;
Jaundice
;
Male
;
Mothers
;
Pediatrics
7.Two Cases of Congenital Asplenia.
Man Chul HA ; Young Tak LIM ; Hi Joo CHUN ; Hi Ju PARK ; Chan Yung KIM
Journal of the Korean Pediatric Society 1987;30(8):916-921
No abstract available.
8.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
Journal of the Korean Pediatric Society 1988;31(3):391-397
No abstract available.
Brain Stem Infarctions*
9.G Deletion Syndrome II.
Bon Su KOO ; Sang Uk PARK ; Yung Tak LIM ; Hee Ju PARK
Journal of the Korean Pediatric Society 1995;38(2):240-244
We experienced a case of G deletion syndrome II in a 8 year and 1 month old boy. He showed mental retardation, microcephaly, high arched palate, low set malformed ears, epicanthal fold, thoracic deformity, tracheomegaly and two lumens of esophagus. Chromosomal study showed the deletion of long arm of chromosome 22, kariotypically he was depicted as 46, XY, 22q-. A brief review of literature was also presented.
Arm
;
Chromosomes, Human, Pair 22
;
Congenital Abnormalities
;
Ear
;
Esophagus
;
Humans
;
Infant, Newborn
;
Intellectual Disability
;
Male
;
Microcephaly
;
Palate
10.Correlation Between Clinical and Pathological Prognositic Factors of IgA Nephropathy in Children.
Hwang Jae YOO ; Bon Su KU ; Eui Jun YANG ; Young Tak LIM ; Su Yung KIM
Journal of the Korean Pediatric Society 1998;41(8):1093-1101
PURPOSE: Clinical and pathological prognostic factors of idiopathic IgA nephropathy have been reported, but mostly in adults and a few in children. Especially studies about correlation between those factors are very rare. METHODS: We studied 58 children patients who were hospitalized to our clinics and diagnosed as IgA nephropathy by renal biopsy from Jan. 1989 to Jun 1996. They got divided into several clinical groups, which are heavy proteinuria group (group A), asymptomatic urinary abnormalities group proteinuria and/or microscopic hematuria (group B), and recurrent gross hematuria group (group C). They are also divided into younger group (younger than 10 years of age) and older group (older than 10 years og age). We compared their pathological findings of bad prognosis, if they have, in different clinical groups. RESULTS: Group A had most pathological factors of bad prognosis such as higher Meadow grade, crescent formation, necrosis, glomerulosclerosis, tubular atrophy, interstitial fibrosis, two or more kinds of immune deposit except IgA, high frequency of electron dense deposits of glomerular capillary wall. Group B treded to have some poor prognostic factors such as tubular atrophy and interstitial fibrosis. in terms of age groups, older group was more apt to be heavily proteinuric than younger group, have such pathological factors of poor prognosis that group A had. CONCLUSION: Heavy proteinuria and relative old age in childhood IgA nephropathy, considered clinically poor prognostic, appears significantly correlated with pathologically poor prognostic factors.
Adult
;
Atrophy
;
Biopsy
;
Capillaries
;
Child*
;
Fibrosis
;
Glomerulonephritis, IGA*
;
Hematuria
;
Humans
;
Immunoglobulin A*
;
Necrosis
;
Prognosis
;
Proteinuria