- Original Article
- Hepatitis associated with Mycoplasma pneumoniae infection in Korean children: a prospective study
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Kyu Won Kim, Jae Jin Sung, Hann Tchah, Eell Ryoo, Hye Kyung Cho, Yong Han Sun, Kang Ho Cho, Dong Woo Son, In Sang Jeon, Yun Mi Kim
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Clin Exp Pediatr. 2015;58(6):211-217. Published online June 22, 2015
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Purpose Mycoplasma pneumoniae (MP) infection is a major cause of respiratory infection in school-aged children. Extrapulmonary manifestations of MP infection are common, but liver involvement has been rarely reported. The aim of this study was to determine the clinical characteristics of MP-associated hepatitis. MethodsThis prospective study included 1,044 pediatric patients with MP infection diagnosed serologically with MP IgM at one medical center... |
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- Hepatitis Complicated with Mycoplasma pneumoniae Infection in Children
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Seung Min Lee, Sung Moon Lee, Hann Tchah, In Sang Jeon, Eell Ryoo, Kang Ho Cho, Yong Han Seon, Dong Woo Son, Hee Joo Hong
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Clin Exp Pediatr. 2005;48(8):832-838. Published online August 15, 2005
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Purpose : Mycoplasma pneumoniae infection is relatively common in childhood. Its extrapulmonary manifestations have been reported so much, but hepatitis associated with it has been reported rarely in Korea.
Methods : A clinical study was performed on 556 patients of M. pneumoniae pneumonia diagnosed serologically at Gil hospital from January 2001 to December 2004. We reviewed 65 cases among these patients,... |
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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
- A Case of Type Ⅰ Glanzmann's Thrombasthenia Diagnosed by Flow Cytometry
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Mun Su Lee, Choong Ho Shin, Kyu Young Kim, Dong Woo Son, Hwa Ryung Chung, Do Hyun Kim
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Clin Exp Pediatr. 1999;42(1):133-137. Published online January 15, 1999
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Glanzmann's thrombasthenia is a rare autosomal recessive hemorrhagic disorder of platelet function with missing or abnormal platelet plasma membrane glycoprotein Ⅱb-Ⅲa, which functions as a receptor for fibrinogen. We have experienced a case of thrombasthenia in a 6-year-old female whose chief complaints were easy bruising, frequent epistaxis, arthralgia and swelling of the right ankle joint. Bleeding time was prolonged in... |
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- 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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- Original Article
- Risk Factors and Outcome of Bronchopulmonary Dysplasia
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Beyong Il Kim, Yun Sil Chang, Dong Woo Son, Hae Kyung Han, Jung-Hwan Choi, Chong Ku Yun, In One Kim, Kyung Mo Yeon, Je G. Chi
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Clin Exp Pediatr. 1994;37(1):78-88. Published online January 15, 1994
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The 45 neonates with bronchopulmonary dysplasia among 355 neonates who were managed with mechanical ventilation and oxygen therapy in NICU of Seoul National University Chhildren's Hospital from January 1, 1968 to December 31, 1991, were analyzed for risk factors and outcome.
The results were as follows:
1) The incidence of bronchopulmonary dysplasia was 12.7%
2) Respiratory Distress Syndrome was most common underlying problem.
3)... |
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- Re-evaluation of TSH Screening TEST in Neonates
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Jin Young Song, Dong Woo Son, Beyong Il Kim, Sei Won Yang, Jung-Hwan Choi, Chong Ku Yoon, Hyung Ro Moon
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Clin Exp Pediatr. 1993;36(11):1502-1506. Published online November 15, 1993
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Five years ago, we made the cut-off value of TSH by dry filter paper method as 15μU/ml to screening congenital hypothyrodism. Since then, 1,210 term neonates, who had no perinatal problems, screening test with this cut-off point. Neonates had been recalled for measurement of serum T4/TSH to rule out congenital hypothyroidism if their TSH value by screening tests reveal more... |
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- A case of acute lymphoblastic leukemia complicating neuroblastoma in remission.
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Dong Woo Son, Bum Soo Park, Jun Jae Kim, Hong Hoe Koo, Hee Young Shin, Hyo Seop Ahn
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Clin Exp Pediatr. 1991;34(5):720-729. Published online May 31, 1991
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As childhood cancer survivors are now increasing in number owing to the improvements in
diagnosis, staging, and treatment, concerns have been raised regarding the quality of survival of these
patients. One of the limitation to quality and length of survival has been the development of second
malignant neoplasm (SMN). In Korea, only one case of SMN has been reported. However, one can
expect that... |
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- A case of hypomelanosis of Ito accompanying ureteral duplication and hypomelanotic scalp hair.
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Dong Woo Son, Beom Soo Park, Heon Seok Han, Hae Il Jung, Yong Choi, Hyung Ro Moon, Seon Hoon Kim, Hwang Choi
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Clin Exp Pediatr. 1991;34(2):281-286. Published online February 28, 1991
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Hypomelanosis of Ito (incontinentia pigmenti achromians) is a cutaneous abnormality consisting of
bizarre, whorly, linear, or patchy hypopigmentation over variable portion of body surface. Multiple
assocaited defects in other systems occur in three quarters of the affected individuals. Most common-
ly, the central nervous system, eye, and musculoskeletal structures are involved. It is suggested that
the cutaneous abnormality, which is often detectable at birth... |
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- IgA Nephropathy in Childhood.
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Yong Choi, Dong Woo Son, Ja Wook Koo, Dong Kyu Jin, Hae Il Cheong, Kwang Wook Ko, Hyun Soon Lee, Yong Il Kim
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Clin Exp Pediatr. 1990;33(9):1237-1243. Published online September 30, 1990
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In this study we compared between the patients with recurrent gross hematuria (group 1, n=45) and
* with nephrotic range proteinuria (group 2, n=21) in IgA nephropathy who were admitted to Seoul
National University Children’s Hospital during the period from January, 1980 to December, 1989.
The results of the study were as follows.
1) Age of onset and sex ratio were not different between the... |
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