- Case Report
- A case of mosaic ring chromosome 13 syndrome
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Soo Young Kim, Soo Min O, Mi Jeong Kim, Eun Song Song, Young Ok Kim, Young Youn Choi, Young Jong Woo, Tai Ju Hwang
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Clin Exp Pediatr. 2009;52(2):242-246. Published online February 15, 2009
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The clinical features of ring chromosome 13 include mental and growth retardation, CNS anomalies, facial dysmorphism, cardiac defects, genital malformations, limb anomalies, skeletal deformities and anal malformations. Although many cases of ring chromosome 13 have been reported worldwide, only 6 cases have been reported in Korea, and the latter cases were not mosaic but pure ring chromosome 13. Here we... |
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- A case of mixed connective tissue disease presenting initially with
Raynaud`s phenomenon
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Soo Young Kim, Young Seok Choi, Young Ok Kim, Young Jong Woo
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Clin Exp Pediatr. 2008;51(8):886-891. Published online August 15, 2008
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Mixed connective tissue disease (MCTD) is characterized by diverse symptoms including rheumatoid arthritis, scleroderma, systemic lupus erythematosus, and dermatomyositis, associated with high titers of antibodies to extractable nuclear antigen (ENA), especially anti-ribonucleoprotein (anti-RNP) antibody. Since the first report of 25 cases with MCTD in adults, there have been only a few cases of MCTD reported in children. Here, we report... |
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- A case of subcutaneous paragonimiasis presented with
pleural effusion
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Soo Young Kim, Sun Ju Park, Si Young Bae, Young Kuk Cho, Chan Jong Kim, Young Jong Woo, Young Youn Choi, Jae Sook Ma, Tai Ju Hwang
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Clin Exp Pediatr. 2008;51(7):760-765. Published online July 15, 2008
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Paragonimiasis is a parasitic infection that occurs following the ingestion of infectious Paragonimus metacercariae from crabs or crayfish. Pulmonary paragonimiasis is the most common clinical manifestation of this infection, but several ectopic paragonimiasis cases have also been reported. Among them, cases of subcutaneous paragonimiasis are rare, especially in children. We report a case of subcutaneous paragonimiasis of the right abdominal... |
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- Original Article
- Alteration of insulin resistance and serum adiponectin levels after one year follow-up of obese children and adolescents
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Min Jee Jeoung, Jung Yeon Shin, Soo Young Kim, Jung Hwa Lee, Kee-Hyoung Lee, Joo Won Lee
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Clin Exp Pediatr. 2007;50(8):767-773. Published online August 15, 2007
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Purpose : Obesity has become a pandemic and especially the prevalence of childhood obesity has increased remarkably over the past years. Childhood obesity is often accompanied by the expected morbidities such as hyperlipidemia, fatty liver and glucose intolerance. We evaluated the pattern of alteration in the body mass index (BMI), serum adiponectin concentration, insulin resistance (HOMA-IR), and complication rates after... |
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- Fluconazole prophylaxis in high-risk, very low birth weight infants
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Soo Young Kim, Soon Joo Lee, Mi Jeong Kim, Eun Song Song, Young Youn Choi
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Clin Exp Pediatr. 2007;50(7):636-642. Published online July 15, 2007
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Purpose : Fluconazole prophylaxis for very low birth weight (VLBW) infants has been shown to reduce invasive fungal infection and its mortality. This study aims to evaluate the effect of fluconazole prophylaxis in VLBW infants on the incidence and mortality of fungal infection.
Methods : VLBW infants with endotracheal intubation and central vascular access admitted to the Neonatal Intensive Care... |
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- Second allogeneic hematopoietic stem cell transplantation in children to overcome graft failure or relapse after initial transplant
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Dong-Yeon Kim, Do Kyun Kim, Soo Young Kim, Seok Joo Kim, Dong Gyun Han, Hee Jo Baek, Hoon Kook, Tai-Ju Hwang
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Clin Exp Pediatr. 2006;49(12):1329-1339. Published online December 15, 2006
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Purpose : Failure of hematopoietic stem cell transplantation(HSCT) may be encountered in practice because of either relapse of the malignancy or dysfunction of the graft. Second HSCT may be the only option for some patients whose initial HSCT failed.
Methods : From May, 1991 to December, 2004, 115 HSCTs were performed at the Pediatric Blood & Marrow Transplantation Center, Chonnam National... |
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- A Study on the Relationship between School-age Obesity and Type of Feeding in Infant Period
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Kyung Lae Cho, Soo Young Kim
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Clin Exp Pediatr. 2005;48(11):1166-1171. Published online November 15, 2005
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Purpose : The aim of this study was to evaluate whether breast milk feeding at infancy has the effect of a programming agent preventing school-age obesity, or whether formula milk feeding is the cause of elementary school-age obesity.
Methods : We randomly selected 4 elementary school in Masan and Changwon city. We calculated the BMI and obesity degree from height... |
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- Efficacy of Antiepileptic Drug on the Benign Childhood Epilepsy with Centro-Temporal Spikes
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Mee Hye Oh, Soo Young Kim, Won Hee Seo, Dae Hun Pee, Byung Min Choi, Baik-Lin Eun
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Clin Exp Pediatr. 2003;46(9):893-897. Published online September 15, 2003
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Purpose : Benign childhood epilepsy with centrotemporal spikes(BECT) is characterized by an excellent prognosis. Therefore, the necessity for the use of antiepileptic drugs is controversial. The object of this study is to know about the long-term follow-up of BECT, comparing daily treatment with antiepileptic drug(AED) versus no medication.
Methods : We retrospectively studied 56 cases of BECTs, examined at Pediatric Neurology... |
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- Depolarization, Repolarization Inhomogeneity and Late Potential after Surgical Repair of Tetralogy of Fallot
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Soo Young Kim, Myung Chul Hyun, Sang Bum Lee, Seung Tae Kim, Jong Soo Lee
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Clin Exp Pediatr. 1999;42(8):1071-1077. Published online August 15, 1999
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Purpose : After repair of tetralogy of Fallot(TOF), ventricular arrhythmia and sudden death remain as serious late complications which are due to right ventricular systolic and diastolic overloading, exposure to hypoxia and surgical scar. Among the various methods for predicting the risk of such complications, we evaluated signal average ECG(SAECG), QRS duration, QT and JT dispersion, cardiothoracic(CT) ratio, age at... |
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- A case of benign recurrent intrahepatic cholestasis.
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Jae Hong Park, Sung Sub Sim, Soo Young Kim, Hee Joo Jeon, Chan Yung Kim
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Clin Exp Pediatr. 1991;34(12):1745-1752. Published online December 31, 1991
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The clinical picture of beingn recurrent intrahepatic cholestasis (BRIC) consists of multiple epi-
sodes of cholestatic jaundice without extrahepatic bile duct obstruction. Since first description by
Summerskill and Walshe in 1959, almost 100 patients with BRIC have been described. The mechanism
involved in the initiation and perpetution of an episode of cholestasis are unknown. Altered bile acid
metabolism has been proposed to play a... |
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- Case Report
- A Case of Epidermolysis Bullosa Letalis.
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Sang Taek Lee, Chang Ho Han, Soo Young Kim, Jung Kwon Lee, Young Dae Kwon, Han Ik Bae
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Clin Exp Pediatr. 1987;30(7):818-825. Published online July 31, 1987
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Epidermolysis bullosa letalis is an uncommon skin disease which is manifest at birth or in infancy.
It is characterized by blister formation occurring spontaneously or after friction or slight trauma.
This blistering disorder has the most severe clinical course, so that death may occur in infancy.
Recently, we experienced a case of epidermolysis bullosa letalis in one day old newborn infant, who
was developed... |
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- A Case of Hand Schuller Christian Disease.
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Yeon Saeng Lee, Soo Young Kim, So Kyung Park, Dong Hak Shin
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Clin Exp Pediatr. 1983;26(4):392-396. Published online April 30, 1983
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Hand-Schuller-Christian disease is reactive granulomatous lesion with histiocytic proliferation,
the cause of which is unknown.
Recently, we experienced a case in a 3 years old female with polydipsia and polyuria.
We established the diagnosis with clinical features, radiologic examination and bone biopsy-
Histiologic examination of frontal bone showed mild to moderate infiltration of eosinophils，
lymphocytes, plasma cells and large histioytes and fibrosis.
Similiar cases reported in... |
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- A Case of Sturge-Weber Syndrome.
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Soo Young Kim, Hyang Sook Kim, Myung Sook Kim, So Young Park, Dong Hak Shin
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Clin Exp Pediatr. 1981;24(11):1111-1115. Published online November 15, 1981
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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... |
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