- Original Article
- A clinical analysis of juvenile dermatomyositis;
focus on clinical manifestations at diagnosis
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So Young Lee, Ji Seok Bang, Hee Seok Kim, Joong Gon Kim
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Clin Exp Pediatr. 2007;50(11):1116-1124. Published online November 15, 2007
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Purpose : Juvenile dermatomyositis (JDM) is the most common of the idiopathic inflammatory myopathies in children. The purpose of this study is to observe demographic, initial presentations, duration of time between disease onset and diagnosis, clinical manifestations and laboratory findings at diagnosis of patients with JDM.
Methods : Forty seven patients identified at Seoul National University Children's Hospital from January 1986... |
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- Case Report
- A Case of Klippel-Trenaunay Syndrome Combinded with Sturge-Weber Syndrome
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Mi Young Kim, So Young Lee, Na Yeon Kim, Sun Ju Lee, Won Duck Kim, Sung Min Cho, Dong Seok Lee, Doo Kwun Kim, Sung Min Choi
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Clin Exp Pediatr. 2003;46(9):909-912. Published online September 15, 2003
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Klippel-Trenaunay syndrome is a rare mesodermal phakomatosis characterized by cutaneous haemangiomata(usually unilateral and involving an extremity), venous varicosities and osseous and soft tissue hypertrophy, of the affected limb. Sturge-Weber syndrome, also a mesodermal pharkomatosis, is characterized by a port-wine nevus, which is present from birth and covers the face and cranium in the territory of the first division of the... |
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- A Case of 21-Monosomy with Holoprosencephaly(Semilobar Type)
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So Young Lee, Sung Min Cho
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Clin Exp Pediatr. 2003;46(8):831-835. Published online August 15, 2003
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Holoprosencephaly of unknown definite causes, has been associated with several chromosome abnormalities involving the autosomes and the sex chromosomes. The most commonly reported associations include dup(3p), del(7q), deletions of chromosome 13, trisomy 13, trisomy 18, and triploidy. In previously reported cases in Korea, none were associated with chromosome 21 anomalies. In conclusion, we reported the first case of holoprosencephaly(semilobar type)... |
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- Case Report
- A Case of Partial Inverted Duplication of Chromosome 7q
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Hyun Ji Kim, So Young Lee, Mi Young Kim, Chung Sun Baek, Won Duck Kim, Dong Seok Lee, Doo Kwun Kim, Sung Min Choi
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Clin Exp Pediatr. 2003;46(5):510-513. Published online May 15, 2003
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Duplication of chromosome 7q has been reported as either partial or complete. Partial 7q duplication was first described by Carpentier in 1972. Pure partial duplication of the long arm of chromosome 7 is extremely rare and only 16 cases with a pure partial duplication of different 7q segment have been described in the literature. Pure partial duplication of the long... |
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- Original Article
- Clinical Study of Status Epilepticus in Children
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So Young Lee, Seung Hee Jung, Yong Kuk Kim, Byung Hak Lim
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Clin Exp Pediatr. 1999;42(2):249-256. Published online February 15, 1999
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Purpose : Convulsive status epilepticus(SE) is a serious, life-threatening neurological condition that requires immediate treatment to avoid significant morbidity and mortality. Despite improvements in the diagnosis and treatment of SE in the last two decades, SE in young infancy is still associated with high morbidity and mortality. Thus, understanding the varied etiology and clinical presentation and prognosis of SE is... |
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- Case Report
- Four Cases of The Imported Falciparum Malariain Childre
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So Young Lee, Tae Sung Ko, Hyun Sook Chi, Young Seo Park
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Clin Exp Pediatr. 1997;40(2):249-253. Published online February 15, 1997
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Malaria is a protozoan disease transmitted by the bite of female Anopheles mosquitoes. Only four species of Plasmodium can infect human, which are P.vivax, P.
ovale, P. malariae, and P. falciparum.
We experienced four cases of the imported falciparum malaria in children who were
admitted due to fever, vomiting, diarrhea, abdominal pain, lethargic state, and/or altered mentality after traveling Kenya and Tanzania without... |
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- Four Cases of Congenital Esophageal Stenosis Due to Tracheobronchial Remnants
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Gi Woong Sung, So Young Lee, Yeon Ho Choi, Kyoung Mo Kim, Jeong Kee Seo, In Won Kim, Kwi Won Park, Jong Je Kim
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Clin Exp Pediatr. 1996;39(2):273-279. Published online February 15, 1996
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Esophageal stenosis due to tracheobronchial remnants is a rare cause of congenital esophageal stenosis. The cause is thought to be esophageal sequestration of tracheobronchial remnants during embryonic separation. Errors in diagnosis are common and high index of suspicion is required for accurate diagnosis, and resection of primary site with anastomosis is recommanded. Although a rare entity, esophageal stenosis due to... |
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- Longterm Follow Up of A Case of Eosinophilic Gastroenteritis
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So Young Lee, Jeong Kee Seo
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Clin Exp Pediatr. 1995;38(1):104-109. Published online January 15, 1995
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Eosinophilic gastroenteritis(EG) is a rare disease characterised histologically by eosinophilic infiltration of the gut wall. The clinical features depend on which layer and location are involved. Patients may be divided into three clinical groups as predominantly mucosal, muscle layer, or subserosal disease based on the histological site of eosinophilic infiltration of the bowel wall, although there is lften considerable overlap.... |
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- A Case of Chronic Granulomatous Disease
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So Young Lee, Dae Chul Kim, Sung Hee Oh, Hahng Lee, Hyang Eun Sohn, Wha Soon Chung, Young Hyeh Ko, Moon Hyang Park
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Clin Exp Pediatr. 1992;35(5):704-712. Published online May 15, 1992
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Chronic granulomatous disease (CGD) is a hereditary disorder of neutrophil with defective killing and digesting of ingested catalase-positive bacteria or fungi in spite of normal phagocytosis. Dissemination of ingested live organisms results in multiple granuloma in reticuloendothelial system and multiple abscesses manifested by recurrent pus-draining suppurative lymphadenopathy, subcutanous abscess, or impetiginous skin rahses, pheumonitis, and hepatosplenomegaly, ultimately resulting in death.
Two... |
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- A Case of Salmonella Group C Meningitis
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Dae Chul Kim, Ju Hyun Han, So Young Lee, Jeh Hoon Shin, In Joon Seol
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Clin Exp Pediatr. 1992;35(10):1449-1453. Published online October 15, 1992
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We experienced a case of salmonella group C meningits in a 3 month old male. His initial chief complaints at the admission were high fever, lethargy, irregular respiration and arrythmias.
Diagnosis was confirmed by lumbar puncture, blood culture and CSF culture. Ceftriaxone was used and recovered with some sequelae such as irritability, generalized spasticity and mild regression of psychomotor development. |
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- Original Article
- A case of report fiber syndrome.
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So Young Lee, Sun Yang Hong, Jae Hoon Shin, In Joon Seol
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Clin Exp Pediatr. 1991;34(1):115-119. Published online January 31, 1991
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This is a report of 10 years old boy whose complete total ophthalmoplegia, ataxia and areflexia
(Fisher syndrome) were the outstanding clinical features. |
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