- Original Article
- Cardiology
- Usefulness of anterior uveitis as an additional tool for diagnosing incomplete Kawasaki disease
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Kyu Jin Lee, Hyo Jin Kim, Min Jae Kim, Ji Hong Yoon, Eun Jung Lee, Jae Young Lee, Jin Hee Oh, Soon Ju Lee, Kyung Yil Lee, Ji Whan Han
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Clin Exp Pediatr. 2016;59(4):174-177. Published online April 30, 2016
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Purpose There are no specific tests for diagnosing Kawasaki disease (KD). Additional diagnostic criteria are needed to prevent the delayed diagnosis of incomplete Kawasaki disease (IKD). This study compared the frequency of coronary artery lesions (CALs) in IKD patients with and without anterior uveitis (AU) and elucidated whether the finding of AU supported the diagnosis of IKD. MethodsThis study enrolled patients diagnosed... |
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- Baseline heart rate variability in children and adolescents with vasovagal syncope
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Sun Hee Shim, Sun-Young Park, Se Na Moon, Jin Hee Oh, Jae Young Lee, Hyun Hee Kim, Ji Whan Han, Soon Ju Lee
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Clin Exp Pediatr. 2014;57(4):193-198. Published online April 30, 2014
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Purpose This study aimed to evaluate the autonomic imbalance in syncope by comparing the baseline heart rate variability (HRV) between healthy children and those with vasovagal syncope. MethodsTo characterize the autonomic profile in children experiencing vasovagal syncope, we evaluated the HRV of 23 patients aged 7-18 years and 20 healthy children. These children were divided into preadolescent (<12 years) and adolescent groups.... |
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- Recent incidence of congenital heart disease in neonatal care unit of secondary medical center: a single center study
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Seon Young Cho, Jin-Hee Oh, Jung Hyun Lee, Jae Young Lee, Soon Ju Lee, Ji Whan Han, Dae Kyun Koh, Chang Kyu Oh
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Clin Exp Pediatr. 2012;55(7):232-237. Published online July 17, 2012
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Purpose With feasibility in the diagnoses of congenital heart disease (CHD) in the antenatal period, we suspect changes have occurred in its incidence. No data have been reported about the current incidence of simple forms of CHD in Korea. We have attempted to assess the recent incidence and characteristics of CHD in the neonatal care unit of a secondary referral medical... |
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- Final height of patients with congenital heart disease
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Soon Ju Lee, Young Kuk Cho, Jae Sook Ma
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Clin Exp Pediatr. 2010;53(2):203-209. Published online February 15, 2010
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Purpose : Growth impairment is usually observed in children with congenital heart disease (CHD). Studies on the final height and weight of this population are insufficient. Our aim was to evaluate the final height of children with CHD and to identify the relationship between CHD and growth.
Methods : We recorded the values of final height and weights of 105 CHD... |
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- Case Report
- A Case of Cystinosis
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Min Ho Jung, Seung On Keun, Soon Ju Lee, Byung Churl Lee
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Clin Exp Pediatr. 2003;46(6):615-619. Published online June 15, 2003
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Cystinosis, an autosomal recessively inherited lysosomal storage disease, results from impaired transport of the amino acid cystine out of cellular lysosomes. The consequent accumulation and crystallization of cystine destroys tissues, causing growth retardation, Fanconi syndrome, renal failure, eye problems, and endocrinopathies. The gene for cystinosis, CTNS, was mapped to chromosome 17p13. The diagnosis of cystinosis was made by measuring the... |
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- Original Article
- Plasma L-Arginine Concentration, Oxygenation Index and Pulmonary Artery Pressure in Premature Infants with
Respiratory Distress Syndrome
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Kyong Ah Jeong, Soon Ju Lee, In Kyung Sung, Chung Sik Chun
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Clin Exp Pediatr. 2003;46(12):1207-1211. Published online December 15, 2003
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Purpose : This study was performed to observe the relationship of plasma L-arginine level and the severity of disease and pulmonary artery pressure in respiratory distress syndrome of premature infants.
Methods : Peripheral blood samples were obtained at 1st, 3rd and 7th day from 21 premature infants with respiratory distress syndrome to analyze the L-arginine concentration. Oxygenation index (OI), an indicator... |
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- Case Report
- A Case of von Gierke Disease
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Young A Joe, Moon Young Song, Bin Cho, Soon Ju Lee, In Kyung Sung, Kyong Su Lee
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Clin Exp Pediatr. 1997;40(12):1756-1760. Published online December 15, 1997
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von Gierke disease(type Ia glycogen storage disease) is an inherited disease associated
with accumulation of glycogen in the liver, kidney, intestine and erythrocytes due to the
defect of glucose-6-phosphatase activity.
Hepatomegaly, doll face, anemia, bleeding tendency and increased susceptability to infection
are common features observed during infancy. Hypoglycemia especially fasting
hypoglycemia is typical metabolic derangement in this disease, followed by metabolic
acidosis, lactic acidemia, hyperlipidemia, hyperuricemia,... |
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