- Case Report
- A Case Report of Acrorenal Syndrome
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Soo Hee Chang, Jo Seph Choi, Soo Chul Cho, Dae Yeol Lee
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Clin Exp Pediatr. 1995;38(8):1151-1154. Published online August 15, 1995
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Acrorenal syndrome is congenital anomaly of the limbs and urinary tract of unknown etiology. Acral malformations consist of varying combinations of oligodactyly, ectrodactyly, syndactyly, brachydactyly, polydactyly, and carpal, tarsal, or metatarsal fusions of the hands and feet. Urinary tract abnormalities include unilateral renal agenesis and duplication of the collecting system. The condition is a polytopic developmental field defect(acrorenal field) and... |
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- Original Article
- Placental Transfer of Anti-H. influenzae Type b Specific IgG and IgG Subclasses
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Soo Hee Chang, Moon Hwan Lee, Pyoung Han Hwang, Soo Chul Cho, Jung Soo Kim
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Clin Exp Pediatr. 1995;38(12):1638-1644. Published online December 15, 1995
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Purpose : Haemophilus injluenzae type b (Hib) is one of the most important causes of invasive bacterial diseases in infants and children. In Korea, however, the proportion occupied by Hib as a cause of pediatric pathogen seems to be less compared to those of western countries.
This study was performed to provide the epidemiologic and immunologic basis of H influenzae type... |
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- Case Report
- A Case of the Renal Artery Aneurysm Associated with the Dysplastic Kidney
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Tae Hee Park, Soo Hee Chang, Young Min Han, Soo Chul Cho, Dae Yeol Lee
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Clin Exp Pediatr. 1995;38(11):1571-1576. Published online November 15, 1995
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Multicystic dysplastic kidney is the most frequent cause of abdominal mass in the neonate. It is frequently associated with contralateral genitourinary tract abnormalities and the most common abnormality is vesicoureteral reflux. Renal artery aneurysm is very rare in the children. Furthermore the case associated with the renal artery aneurysm has not been reported yet.
We experienced a case of the left... |
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- A Case of Wiskott-Aldrich Syndrome
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Byoung Geun Lee, Soo Hee Chang, Soo Young Cho, Pyoung Han Hwang, Jung Soo Kim
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Clin Exp Pediatr. 1994;37(11):1615-1619. Published online November 15, 1994
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Wiskott-Aldrich Syndrome is an X-linked disorder characterized by recurrent infection, thrombocytopenia and eczema. Various defects in cell-mediated immunity and deficient antibody response to carbohydrate antigens have been described. We experienced a case of Wiskott-Aldrich Syndrome of 28 months old male patient. He has been suffered from multiple petechiae with bleeding, recurrent pyogenic infections and generalized eczema since 3 months of... |
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