• Search
  • Advanced Search

Search

  • HOME
  • Search
Original Article
Clinical Analysis of Pediatric Death Patients Visiting Emergency Center
Do Hyun Kim, Seong Hun Lee, Sang Bae Lee, Min Hyuk Ryu, Dong Jin Lee
Clin Exp Pediatr. 2004;47(1):12-17.   Published online January 15, 2004
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...
Case Report
A Case of Type Ⅰ Glanzmann's Thrombasthenia Diagnosed by Flow Cytometry
Mun Su Lee, Choong Ho Shin, Kyu Young Kim, Dong Woo Son, Hwa Ryung Chung, Do Hyun Kim
Clin Exp Pediatr. 1999;42(1):133-137.   Published online January 15, 1999
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...
Pena-Shokeir I Syndrome in a Newbonrn Infant
Myung Gil Han, Kyu Young Kim, Dong Woo Son, Bo Young Yoon, Kyung Hee Park, Do Hyun Kim, Hyung Ro Moon
Clin Exp Pediatr. 1997;40(5):721-725.   Published online May 15, 1997
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...
Herditary Anhidrotic Ectodermal Dysplasiain Twins
Myung Gil Han, Do Hyun Kim, Hyung Ro Moon
Clin Exp Pediatr. 1996;39(7):1005-1009.   Published online July 15, 1996
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...
Original Article
An Agiographic Study on Developemental and Spatial Relationship of Patent Ductus Arteriosus (PDA) and Aortic Arch in Right Ventricular Outflow Tract (RVOT) Obstruction.
DO Hyun Kim, Youn Mo Ahn, Ha Balk Lee, Kyoo Hwan Rhee, Hahng Lee, Seok Chol Jeon
Clin Exp Pediatr. 1988;31(9):1139-1145.   Published online September 30, 1988
Ductus arteriosus plays important hemodynamic role in fetal development, and establish a certain spatial relationship with aorta. Although ductus arteriosus normally closes after birth, it could remain patent alone, or in association with various congenital heart anomalies. In these patients the develop- mental hemodynamic changes may result in the specific variation in the spatial relationhip of patent ductus arterisus (PDA) and aortic arch. The developmental...
Clinical Characteristics and Pathogenesis of Typhlitis in Childhood Non-Lymphocytic Leukemia-Considerations on Clinical Mangement with Report of Two Cases and Literature Review.
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
Clin Exp Pediatr. 1988;31(5):607-620.   Published online May 31, 1988
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...
Cineaortography by Countercurrent Injection via the Radial Artery in Neonates and Infants.
Do Hyun Kim, Hong Kun Kim, In Joon Seol, Kyoo Hwan Lee, Goo Hwan Je
Clin Exp Pediatr. 1987;30(7):716-721.   Published online July 31, 1987
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....