- Original Article
- Neurology
- Comparison of conservative therapy and steroid therapy for Bell’s palsy in children
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Hye Won Yoo, Lira Yoon, Hye Young Kim, Min Jung Kwak, Kyung Hee Park, Mi Hye Bae, Yunjin Lee, Sang Ook Nam, Young Mi Kim
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Clin Exp Pediatr. 2018;61(10):332-337. Published online September 12, 2018
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Purpose: Bell’s palsy is characterized by sudden onset of unilateral facial weakness. The use of corticosteroids for childhood Bell’s palsy is controversial. This study aimed to identify clinical characteristics, etiology, and laboratory findings in childhood Bell’s palsy, and to evaluate the efficacy of corticosteroid treatment.
Methods: We conducted a retrospective analysis of children under 19 years of age treated for Bell’s... |
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- Venous angioma may be associated with epilepsy in children
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Bo Ryung Kim, Yun Jin Lee, Sang Ook Nam, Kyung Hee Park
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Clin Exp Pediatr. 2016;59(8):341-345. Published online August 24, 2016
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Purpose Venous angioma (VA) is the most common congenital abnormality of the intracranial vasculature. This study aimed to investigate the relationship between VA and epilepsy and to identify the characteristics of children with VA and epilepsy. MethodsThe records of all patients aged less than 18 years who underwent brain magnetic resonance imaging (MRI) at Pusan National University Hospital were retrospectively reviewed. Patients... |
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- Needle aspiration as therapeutic management for suppurative cervical lymphadenitis in children
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Mee Young Baek, Kyung Hee Park, Ju Hee We, Su Eun Park
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Clin Exp Pediatr. 2010;53(8):801-804. Published online August 31, 2010
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Purpose This study aimed to evaluate the usefulness of the needle aspiration alternative to open surgical drainage of children with suppurative cervical lymphadenitis requiring surgical drainage. MethodsFrom January 1998 to June 2008, we retrospectively reviewed 38 children treated with needle aspiration as management with suppurative cervical lymphadenitis instead of open surgical drainage. ResultsAll 38 children underwent only 1 puncture. Two patients (5.2%) out... |
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- Detection of HHV6 and EBV in histiocytic necrotizing lymphadenitis
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Kyung Hee Park, Sung Shik Park, Ji Yeon Kim, Su Eun Park
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Clin Exp Pediatr. 2008;51(9):987-991. Published online September 15, 2008
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Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis (HNL), is a self-limited disease characterized by cervical lymphadenopathy and fever. The etiology of KFD remains unknown; however, the self-limiting nature of HNL suggests the cause of this disease could be viral infection. For this reason, several viruses have been evaluated as possible etiologies of HNL, including Epstein-Barr virus (EBV), human... |
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- Congenital Chloride Diarrhea in 5 Korean Infants
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Dong Hun Rhie, Sun Hwan Bae, Ji Eun Choi, Bo Young Yun, Dong Woo Son, Choong Ho Shin, Kyung Hee Park, Jae Sung Ko, Jeong Kee Seo
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Clin Exp Pediatr. 2000;43(11):1465-1472. Published online November 15, 2000
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Purpose : Congenital chloride diarrhea(CLD) is an autosomal recessive disease characterized by life-long watery diarrhea of prenatal onset with high fecal Cl－ concentration. Recent studies have revealed that the protein product of the down-regulated in adenoma(DRA) gene is an intestinal anion transporter molecule and causes CLD when mutated. We investigated the clinical characteristics of CLD in Korean infants in order... |
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- Case Report
- Pena-Shokeir I Syndrome in a Newbonrn Infant
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Myung Gil Han, Kyu Young Kim, Dong Woo Son, Bo Young Yoon, Kyung Hee Park, Do Hyun Kim, Hyung Ro Moon
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Clin Exp Pediatr. 1997;40(5):721-725. Published online May 15, 1997
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Pena-Shokeir I syndrome is a multiple malformation syndrome displaying characteristics of camptodactyly, multiple ankylosis, severe muscle weakness, facial anomalies (low set ears, hypertelorism, depressed tip of nose), polyhydramnios, fetal growth retardation & pulmonary hypoplasia which are inherited by autosomal recessive trait.
We experienced 1 case of Pena-Shokeir I syndrome in a neonate (41 weeks, 2.08Kg). This patient suffered from dyspnea. Respiratory... |
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- A Case of Chéiak-Higashi Syndrome
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Soo Jin Kim, Soo Kyung Choi, Kyung Hee Park, Ghee Young Jung, Young Ok Lee
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Clin Exp Pediatr. 1995;38(7):983-987. Published online July 15, 1995
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Chéiak-Higashi syndrome is a rare autosomal recessive disease characterised by partial oculocutaneous albinism, frequent pyogenic infections and abnormal large lysosomal granules in leukocytes and other granule containing cells.
We experienced a case of Chéiak-Higashi syndrome in a twenty days old male who show-ed partial albinism, recurrent infections and characteristic abnormal large granules in granuloc-ytes on peripheral blood smear and bone marrow... |
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- A Case of Intestinal Lymphangiectasia
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Yae Kyung Suh, Kyung Hee Park, Chul Ho Jang, Bum Soo Park, Jeong Kee Seo, Sung Hae Park, Je Geun Chi, Kyung Mo Yeon, Kwi Won Park
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Clin Exp Pediatr. 1992;35(12):1737-1743. Published online December 15, 1992
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Intestinal lymphangiectasia is a primary or secondary disorder of the gastrointestinal tract, which is associated with lymphatic dysfuction and protein-losing enteropathy. It's clinical manifestations vary widely, but the main symptoms are abdominal distention, edema, abdominal pain and growth failure.
We described a 15-yr-old boy, who suffered from above symptoms since third year of his age and diagnosed by duodenal endoscopy which... |
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- Original Article
- Quantitative Assessment of the Diameters of Tricuspid Valve, Mitral Valve and Great Arteries in the Normal Human Fetus -Cross Sectional Echocardiographic Study-
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Jung Yun Choi, Kyung Hee Park, Chung Il Noh, Yong Soo Yun, I Seok Kang, Eun Sook Han
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Clin Exp Pediatr. 1992;35(11):1566-1572. Published online November 15, 1992
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In order to assess the growth of the mitral valve, tricuspid valve, and the aortic and pulmonary pathways in the normal human fetus, 181 fetal echocardiograms taken from 127 pregnant women (some women had repeated examinations) were analysed.
Diameters were measured from cross sectional images and were correlated with gestational period. The diameter ratios of tricuspid valve/mitral valve, aorta/main pulmonary artery,... |
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- A Case of Acute Renal Failure Associated with Rhabdomyolysis in Carbon Monoxide Intoxication.
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Kyung Hee Park, Sei Hee Hwang, Hae Il Cheong, Yong Choi, Kwang Wook Ko
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Clin Exp Pediatr. 1990;33(5):690-694. Published online May 31, 1990
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We experienced a case of acute renal failure associated with rhabdomyolysis after Carbon
Monoxide intoxication in a 12 year old Korean girl who had marked soft tissue swelling of the left
thigh, reddish brown colored urine and oliguria.
Diagnosis was made by clinical features, markedly elevated serum muscle enzymes and serum
myoglobin, and Tc 99m-MDP bone scan which revealed increased radioactivity at the left... |
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- Clinical Consideration of Coarctation of the Aorta.
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Jong Woon Choi, Kyung Hee Park, Jung Yun Choi, Yong Soo Yoon
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Clin Exp Pediatr. 1990;33(5):651-657. Published online May 31, 1990
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A retrospective analysis of clinical findings in 98 patients with coarctation of the aorta who visited
Department of Pediatrics of Seoul National University Hospital from 1980 till 1988 was performed.
1) The most common age group was under 1 year of age (58 case; 59.2%), and male-to-female ratio
was 1.58:1.
2) The common symptoms and signs were dyspnea/ tachypnea, hepatomegaly and chest wall
retraction. Congestive heart failure... |
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