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Sung Il Ahn 7 Articles
Original Article
Two Cases of Congenital Dislocation of the knee.
Hwa Jin Byun, Hye Kyung Lee, Hee Ju Kim, Sung Il Ahn, Chang Soo Ra, Woo Ku Chung
Clin Exp Pediatr. 1990;33(3):404-409.   Published online March 31, 1990
Congenital dislocation of the knee is rare deformity. Since its first description by chatelaine in 1822, many authors have been proposed. The authors experienced two cases of congenital dislocation of the both knees and a brief review of the related literatures was made.
The Incidence of Undescended Testes at Birth.
Chong Koo Chong, Wan Chol So, Byong Lyol Lee, E Boong Kwon, Sung Il Ahn
Clin Exp Pediatr. 1984;27(7):673-677.   Published online July 31, 1984
We examined 1,226 male neonates in order to discover how often the testicle was undescended at birth during the 18months period from Mar. 1982 through Aug. 1983. The following results were obtained: 1)We found undescended testes in 124(10.1%) of them. 2)In babies of less than 37 weeks gestation the incidence was 39.4% whereas in those of 37 weeks or more...
Case Report
Sonography in the Diagnosis and Management of Hydrops of the Gallbladder in Childern with Mucocutaneous Lymph Node Syndrome.
Byung Lyul Lee, Byung Hwan Lee, Kwang Chan Doh, Sung Il Ahn
Clin Exp Pediatr. 1982;25(6):633-637.   Published online June 30, 1982
Acute hydrops of the gallbladder is described in one patient who had mucocutaneous lymph node syndrome. During the course of her illness, acute addominal pain, vomiting and right upper guadrant tenderness were developed. Diagnosis was readily made with ultrasonography, and the patient was followed with this te-chnique. We managed her conventionally without surgical intervention. The galbladder returned to normal size...
A case of Lacunar Skull.
Byung Lyul Lee, Byung Hwan Lee, Kwang Chan Doh, Sung Il Ahn
Clin Exp Pediatr. 1982;25(5):508-511.   Published online May 31, 1982
A case of lacunar skull, female newborn infant, associated with skin defect on the lumbosacral region, spina bifida, meingomyelocele and paraplegia is reported. Hydrocephalus developed eventually. Diagnosis was made by X-ray of skull. The roentgenographic apperance shows typhical a soap bubble texture or irregular patches of rarefaction. A brief review of the related literature is given.
Poststreptococcal Glomerulonephritis without Abnormality of Urine.
Byung Hwan Lee, Byung Lynl Lee, Kwang Chan Doh, Sung Il Ahn, Hyun Soon Lee
Clin Exp Pediatr. 1982;25(10):1073-1077.   Published online October 31, 1982
A case is presented of a 15-year old girl with clinical and laboratory findings Strongly suggestive of poststreptococcal glomerulonephritis but without abnormalities in the urine. Repeated examinations of the urine demonstrated absence of proteinuuria and hematuria throughout a nineteen-day hospital course. Her renal biopsy specimen revealed small scattered intramembranous, subendothelial and mesangial deposits in. immunofluorescence and electron microscopy, but essentially normal pattern in light microscopy indicating...
Ai Lan Kim, Hwa Jung Yoon, Byung Lyul Lee, Whan Kok Yong, Sung Il Ahn
Clin Exp Pediatr. 1980;23(7):578-581.   Published online July 15, 1980
A case of a achondroplasia in a 6 month-old-boy was presented with a brief review of the literature. He was admitted with the chief complaints of frequent respiratory infections, and stunted growth. This baby showed stunted growth, short arms and legs, prominent forehead, flatening of the bridge of the nose, and moderate degree of kyphosis. All laboratory datas were nomal....
Cornelia de Lange Syndrome.
Hwa Jung Yoon, Ai Lan Kim, Whan Kok Yong, Sung Il Ahn
Clin Exp Pediatr. 1980;23(6):479-485.   Published online June 15, 1980
The Cornelia de Lange syndrome is characterized by severe growth and mental retardations and a cluster of minor malformations, the facial appearance being most characteristic. In the present paper, we shall report I case of this syndrome in Korean male infant and the variability of de Lange syndrome is discussed. The bady showed hirsutism, low forehead coved with lanugo-like hair,...
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