1.A Case of Congenital Hypofibrinogenemia.
Ji In PARK ; In Seok LIM ; Chul Ha KIM ; Byoung Hoon YOO
Journal of the Korean Pediatric Society 1990;33(7):1009-1011
No abstract available.
2.Asymptomatic human rotavirus infections during infancy and preschool period.
Hye Lim JUNG ; Byoung Hoon YOO ; Tae Sub SHIM
Journal of the Korean Pediatric Society 1989;32(11):1482-1488
No abstract available.
Humans*
;
Rotavirus Infections*
;
Rotavirus*
3.Echocardiographic Evaluation of Sequential Change of Cardiac Function in Normal Neonates.
Ji In PARK ; Chul Ha KIM ; Byoung Hoon YOO
Journal of the Korean Pediatric Society 1990;33(11):1533-1539
No abstract available.
Echocardiography*
;
Humans
;
Infant, Newborn*
4.A Case of Pulmonary Lymphangiectasis Associated with Chylothorax.
Min Hee KIM ; Jae Kyoung LEE ; Oh Bae CHUN ; Byoung Hoon YOO ; Jae Hyung YOO
Journal of the Korean Pediatric Society 1987;30(4):422-426
No abstract available.
Chylothorax*
;
Lymphangiectasis*
5.The Influence of Valproic acid and Carbamazepine on the Immunologic Status of Children.
Byoung Young LIM ; Soo Ahn CHAE ; Byoung Hoon YOO
Journal of the Korean Child Neurology Society 1999;6(2):293-298
PURPOSE: Antiepileptic drug (AED) therapy has been reported to induce immunological alterations in epileptic patients. However, despite extensive studies, the accumulated data are not consistent and there is still confusion and controversy over the effects of AEDs on the immune system. This study tries to elucidate the effects of anticonvulsant on some immune parameters, and serum concentration of IgA, IgG, IgM. METHODS: Thirty pediatric epileptic patients[Group A (n=12) : patients on carbamazepine, Group B (n=10) : patients on valproic acid and Group C (n=8) : patients on carbamazepine and valproic acid] were enrolled in this study and the levels of IgA, IgG, and IgM were determined before treatment and after 10 months of anticonvulsant therapy. Paired t-test was used to evaluate the data. p values<0.05 were considered significant. RESULTS: The mean serum concentratrions of IgG was elevated in patients receiving anticonvulsants (p<0.05) but mean concentrations of IgA and IgM were not different significantly. CONCLUSION: Our results demonstrate that anticonvulsants elevate the serum concentrations of IgG level, suggesting that anticonvulsants may increase humoral immunity and decrease the opportunity of infectious disease, thus decreasing the convulsion.
Anticonvulsants
;
Carbamazepine*
;
Child*
;
Communicable Diseases
;
Humans
;
Immune System
;
Immunity, Humoral
;
Immunoglobulin A
;
Immunoglobulin G
;
Immunoglobulin M
;
Seizures
;
Valproic Acid*
6.Clinical Analysis of Serum and Urine N-Acetyl-B-D-Glucosaminidase(NAG) in Renal Disease.
Yo Han CHUNG ; In Seok LIM ; Chul Ha KIM ; Byoung Hoon YOO ; Tae Sub SHIM
Journal of the Korean Pediatric Society 1994;37(3):383-389
Recently, NAG activity has gained increasing importance as and aid in the diagnosis of renoparenchymal diseases. Elevation of urine NAG activity has been found to be an indicator of renoparenchymnal diseases. To evaluate the diagnostic value of the NAG activity test in the renal disease, we carried out clinical study on 31 cases of renal disease patients who had been admitted to the Department of Pediatrics, Chung-Ang University Hospital between March 1992 and February 1993. We analyese by two data: (1) Stastical Package for the Social Science. (2) Students'T test. The results were as follows 1) The urine NAG activity significantly increased (p<0.05) to 69.9+/-5165.69U/hr/mg Creatinine (U/hr/mg Cr) in the renal disease group compared to 3.6+/-1.91U/hr/mg Cr in the control group. 2) The serum NAG activity was 11.69+/-5.18U/L in the renal disease group and 10.58+/-4.04U/L in the control group. There was no significant difference in the serum NAG sctivity between two groups. 3) In the renal disease group, the serum NAG activity was 10.78+/-3.32U/L in male 12.53+/-6.47U/L in female. There was no significant difference between both sexes. In the renal disease, the urine NAG activity was 33.62+/-30.67U/hr/mg Cr in male and 114.05+/-241.62U/hr/mg Cr female. There was no significant difference between both sexes (p<0.05). 4) In the renal disease group, the urine NAG activity increased 314.73+/-420.39U/hr/mg Cr in the 2 years old group but there was no significant difference of urine NAG activity compared to above 2 years old group . 5) The urine NAG activities were 93.1+/-0193.04U/hr/mg Cr in the poteinuria subgroup and 13.3+/-47.62U/hr/mg Cr in the nonproteinuria subgroup and 3.66+/-1.91U/hr/mg Cr in the control group. There was no significant difference between the proteinuria subgroup and the nonproteinuria subgroup. but there was significant difference between nonproteinuria subgroup and control grouop(p<0.005).
Child, Preschool
;
Creatinine
;
Diagnosis
;
Female
;
Humans
;
Male
;
Pediatrics
;
Proteinuria
;
Social Sciences
7.The effect of Large for Gestational Age on Asymmetrical Ventricular Septal Hypertrophy in the Newborn.
Yong Soo KIM ; Soo Ahn CHAE ; In Seok LIM ; Byoung Hoon YOO
Journal of the Korean Society of Neonatology 1998;5(1):40-44
PURPOSE: It has been known for a long time that infants of insulin dependent diabetic mothers are prone to develop macrosornia, organomegaly, hyperbilirubinemia, respiratory distress syndrome, hypoglycemia, hypocalcemia, septicemia and congenital anomalies in the neonatal period. And echocardiographic asymmetrical- ventricular septal hyper- trophy(ASH) has been observed in the newborn infants of diabetic mothers. The etiology of the ASH remains unknown, although fetal hyperglycemia and subsequent glycogen deposits have been postulated as contributing factors. Therefore, we have studied whether large for gestational age(LGA) has played an important role of developing ASH. METHODS: We compared echocardiographic findings in neonates of LGA and appro- priate for gestational age(AGA), who were admitted to the Department of Pediatrics, Chung Ang University Hospital from April 1994 to March 1997. RESULTS: 1) Mean LVED in LGA and AGA were 1.96+0.06cm and 1.94+0.04cm, respectively. 2) Mean LVPW in LGA and AGA were 0.37+0.05cm and 0.370.05cm, respectively. 3) Mean IVS in LGA and AGA were 0.400.09cm and 0.380.09cm, respectively. 4) Mean IVS/ LVPW in LGA and AGA were 1.09+0.12 and 1.040.17, respectively. There was no statistical significance between two groups in echocardiographic findings. CONCLUSION: There is no relation between LGA and ASH in the neonate. According- ly, we may not need to perform echocardiography LGA routinely.
Echocardiography
;
Gestational Age*
;
Glycogen
;
Humans
;
Hyperbilirubinemia
;
Hyperglycemia
;
Hypertrophy*
;
Hypocalcemia
;
Hypoglycemia
;
Infant
;
Infant, Newborn*
;
Insulin
;
Mothers
;
Pediatrics
;
Sepsis
8.A Case of Idiopathic Long QT Syndrome with 2:1 Atrioventricular Block.
Kwang In LEE ; Chul Ha KIM ; In Seok LIM ; Dong Keun LEE ; Byoung Hoon YOO
Journal of the Korean Pediatric Society 1995;38(12):1701-1705
No abstract available.
Atrioventricular Block*
;
Long QT Syndrome*
9.Primary Cutaneous B Cell Lymphoma.
Hak Kyu LEE ; Yoon Whoa CHO ; Kye Yong SONG ; Byoung Hoon YOO ; Byung In RO
Annals of Dermatology 1995;7(1):58-61
A 7-year-old girl had a 7 × 6cm sized dark red colored tumor on the left elbow and several erythematous macules on the face, right upper arm, and both thighs. Her general health was good and all laboratory findings were within normal limit. Histopathologic examination revealed an infiltration of atypical mononuclear cells in the dermis and subcutis. L26 and leukocyte common antigen were positively stained in an immunohistochemical study. According to clinical, histological and immunohistochemical findings, we diagnosed the disease as primary cutaneous B cell lymphoma. The patient's skin lesions markedly improved after a surgical excision and chemotherapy.
Antigens, CD45
;
Arm
;
Child
;
Dermis
;
Drug Therapy
;
Elbow
;
Female
;
Humans
;
Lymphoma, B-Cell*
;
Skin
;
Thigh
10.A Case of Laurence-Moon-Biedl Syndrome Including Diabetic Mellitus.
Byoung Hoon LEE ; Byung Rai CHO ; Myoung Ik LEE ; Keun Chan SOHN ; Hyung Joon YOO
Journal of the Korean Pediatric Society 1989;32(6):857-861
No abstract available.
Laurence-Moon Syndrome*