- Case Report
- A Case Report of Autoimmune Hepatitis Associated with Choledochal Cyst and Pancreatitis
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Kyung Ran Park, Sun Young Lee, Soon Young Kim, Hyoung Shim Chang, Nam Su Back, Chong Jai Kim, Joong Gon Kim, Jeong Kee Seo
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Clin Exp Pediatr. 1996;39(8):1146-1150. Published online August 15, 1996
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Autoimmune hepatitis in children is a rare and severe inflammatory disease of unknown
etiology, and progress to cirrohosis and liver failure, generally is responsive to immunosuppressive
therapy. It is more prevalent in women than men, and characterized by the presence of
circulating autoantibodies, a high serum globulin. Extrahepatic manifestations such as thyroiditis,
ulcerative colitis, glomerulonephritis and autoimmune hemolytic anemia, are associated.
We report, to our... |
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- One Case of Aneurysm of Vein of Galen
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Sun Young Lee, Jong Won Lee, Dong Joo Shin, Jin Keun Bang, Du Bong Lee, Kwang Woo Lee
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Clin Exp Pediatr. 1994;37(7):1011-1015. Published online July 15, 1994
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Aneurysm of the vein of Galen is a rare midline arteriovenous malformation, usually presenting with cardiac failure in infancy or with hydrocephalus and raised intracranial pressure in older children.
We experienced a case of the vein of Galen aneurysm diagnosed with computed tomographic (CT) features and magnetic resonance image(MRI), a new imaging modality. Our case was a 3 day-old male neonate... |
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- A Case of Kugelberg-Welander Syndrome
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Sun Young Lee, Myung Ik Lee, Soon Wha Kim, Don Hee Ahn, Je Geun Chi
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Clin Exp Pediatr. 1992;35(9):1263-1266. Published online September 15, 1992
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We have experienced a 6 year-old female patient who had suffered from progressive muscular atrophy with weakness and loss of voluntary motor action since 3 years of age. She was diagnosed as Kugelberg-Welander syndrome by EMG and muscle bio. Multiple polyphasic motor unit potentials were revealed on EMG and grouped muscle atrophy without fibrosis or degenerative change was found on... |
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- Seven Cases of Immotile Cilia Syndrome
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Sun Young Lee, Myung Ik Lee, Don Hee Ahn, Keun Chan Sohn, Je Geun Chi
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Clin Exp Pediatr. 1992;35(8):1127-1134. Published online August 15, 1992
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Immotile cilia syndrome is a disease caused by congenital abnormality of the cilia and symptom complex composed by chronic rhinitis, sinusitis, otitis, male infertility etc.
We have experienced 7 cases of immotile cilia syndrome diagnosed by electron microscopic finding of nasal or bronchial mucosal biopsies since 1984. Six cases were girls and type Id was most common (4 cases) on... |
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