- Original Article
- Clinical Analysis of Pediatric Death Patients Visiting Emergency Center
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Do Hyun Kim, Seong Hun Lee, Sang Bae Lee, Min Hyuk Ryu, Dong Jin Lee
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Clin Exp Pediatr. 2004;47(1):12-17. Published online January 15, 2004
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Purpose : We analyzed pediatric death patients who visited Dong-Kang Hospital emergency center, in order to minimize unexpected pediatric deaths.
Methods : The authors analyzed retrospectively the medical records of 110 pediatric patients who died before and within 24 hours after admission to the emergency center of Ulsan Dong-Kang General Hospital from January 1997 to December 2002.
Results : We classified three... |
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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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- Herditary Anhidrotic Ectodermal Dysplasiain Twins
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Myung Gil Han, Do Hyun Kim, Hyung Ro Moon
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Clin Exp Pediatr. 1996;39(7):1005-1009. Published online July 15, 1996
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Hereditary anhidrotic ectodermal Dysplasia is a congenital disease displaying characteristics of
anhidrosis, hypotrichosis and dental defect which are caused by developmental anomaly of
ectodermal epidermis and its appendages.
We experienced two cases of hereditary anhidrotic ectodermal dysplasia in two-year and
four-month old twin brothers. These patients suffered from intermittent high fever early in life
which brought them to our clinical attention. However the diagnosis of... |
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- Clinical Characteristics and Pathogenesis of Typhlitis in Childhood Non-Lymphocytic Leukemia-Considerations on Clinical Mangement with Report of Two Cases and Literature Review.
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Do Hyun Kim, Sung Oh Kim, Soo Yup Lee, In Joon Seol, Hahng Lee, Chong Moo Park, Poong Man Jung, Seok Chol Jeon, Young Hyeh Ko, Jung Dal Lee
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Clin Exp Pediatr. 1988;31(5):607-620. Published online May 31, 1988
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The treatment of acute leukemia in childhood has been increasingly successful due to progression
of chemotherapeutics and other supportive care. Improved survival rates in acute childhood leukemia
have been associated with an increasing number of complications in the gastrointestinal tract.
Typhlitis also known as ileocecal syndrome is a necrotizing inflammation of the cecum in leukemic
patients on chemotherapy in the terminal stage of the... |
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- Cineaortography by Countercurrent Injection via the Radial Artery in Neonates and Infants.
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Do Hyun Kim, Hong Kun Kim, In Joon Seol, Kyoo Hwan Lee, Goo Hwan Je
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Clin Exp Pediatr. 1987;30(7):716-721. Published online July 31, 1987
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Cineaortography by countercurrent injection via the radial artery was performed for the diagnosis
of aortic arch anomalies in four infants with congenital heart anomalies. A patent ductus arteriosus,
a hypoplastic pulmonary arteries and a normal aortic arch were demonstrated respectively by this
method. The complete obstruction at the site of shunt operation for tricuspid atresia type lb was
confirmed in the post operative period.... |
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