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Case Report
A Case of Letter-Siew Disease.
Yoon Ho Kang, Suck Young Lee, Jin Sook Lee, Kwang Ho Kim, Soo Nam Lee
Clin Exp Pediatr. 1985;28(10):1032-1036.   Published online October 31, 1985
A case of Letterer-Siwe disease in a 6 month-old Korean male manifesting maculopapular skin rash, watery diarrhea, fever and bony skull defect as classical features of the disease was presented. The diagnosis was confirmed by clinical symptoms, histopathologic and radiologic findings. The authors report a fatal case which was treated in hospital with intensive antibiotics, corticosteroid and alkylating agent.
A Case of Fanconi's Anemia.
Dong Hwan Cha, Jung Shim Choi, Kwang Ho Kim, Hong Ku Lee, Sha Sook Hahn
Clin Exp Pediatr. 1983;26(8):808-811.   Published online August 31, 1983
Recently we experienced a case of Fanconist anemia in a 6 years old male child and reported with brief reviews of literatures. The initial symptom was nasal bleeding and pallor which observed between age of 4 years to 6 years. He was microcephaly, His both thumbs were rudimentary. Cystogenic study showed chromosomal breakage. Bone marrow study showed hypocellularity.
A Case of Weismann-Netter Stuhl Syndrome.
Kwang Ho Kim, Hong Ku Lee, Dong Hwan Cha, Jung Sim Choi, Chie Ja Cho, Jung Sook Lee
Clin Exp Pediatr. 1983;26(6):622-625.   Published online June 30, 1983
Weismann-Netter-Stuhl syndrome is congenital anterior bowing of the diaphyses of the tibia and fibula usually bilateral and symmetical, which is clinically resembles the sabre shin of syphilis. A case of Weismann-Netter-Stuhl syndrome in a 5 years oldboy was presented with a brief review of literature. This boy showed stunted growth, anterior bowing of legs and moderate degree of dyphosis, clear intelligence. X-ray showed...
A case of lamellar ichthyosis.
Dong Whan Cha, Kwan Sup Chung, Kwang Ho Kim, Duk Hyun Kim
Clin Exp Pediatr. 1982;25(9):967-971.   Published online September 30, 1982
One case of rare form of lamellar ichthyosis was reported. On admission, the entire skin surface of this infant was covered with parchment-like membrane especially below both ears and extensor surface of upper arms. Masked face, eversion of both lips and fixed semiflexion attitude of the upper limbs were also noted. Diagnosis of lamellar ichthyosis was made by clinical features, histcpathological and laboratory studies. A brief review...
Original Article
Changes in Serum Complement and Immunglonulins following Cardiopulmonary Bypass.
Hong Jin Kim, Jun Hee Sul, Sung Kyn Lee, Dong Shik Chin, Kwang Ho Kim, Pill Whoon Hong
Clin Exp Pediatr. 1982;25(8):781-786.   Published online August 31, 1982
Clinical problem occuring in the early post operative period after cardiopulmonary bypass may ne related to the altered function of capillary bed which was affected by activation of complement system. This is so called post perfusion syndrome. We selected 20 patients with confirmed congenital heart disease by cariac catheterization. We studied the changes in the C3 , immunolglobulins, total protein,...
Case Report
A Case of Gastric Teratoma Combined with Congenital Syphilis.
Du Yung Lee, Jin Sook Lee, Dong Whan Cha, Se Jin Kang, Kwang Ho Kim, Kwan Sub Chung
Clin Exp Pediatr. 1982;25(4):404-409.   Published online April 30, 1982
Gastric Teratomas are exetremely rare in infancy and childhood. About 50 cases of gastric teratomas are reported in the world's literature. Most of them were male. Few were dignosed prior to surgery. The mos thelpful diagnostic aid was of teeth or bone in radiologic examinations. Treatment is surgical excision and all of them were benign. Recently, we experienced a case...
Original Article
Clinical Analysis of Cord Serum Immunoglobulin M.
Duk Jin Yun, Kwang Ho Kim, Kwan Sub Chung, Gui Nyung Lee
Clin Exp Pediatr. 1981;24(6):517-524.   Published online June 15, 1981
Determination of the immunoglobulin M(IgM) in umbilical cord sera has been advocated as a screening test for intrauterine infection, since the IgM is produced by the fetus and is not transported across the placenta from mother. The low level of IgM in normal neonate is thought to reflect the infrequent encounter of antigenic stimuli by the futus, upon exposure to...
Clinical Analysis of Short Stature.
Kwang Ho Kim, Hak Yong Kim, Duk Hi Kim, Duk jin Yun
Clin Exp Pediatr. 1980;23(9):702-709.   Published online September 15, 1980
Adequate growth is the most importment and principal factor in the fields of pediatrics and also it is great concern to all parents. There are many causes of short stature, secondary to a variety of causes. Clinical evaluation of short stature requires a wide variety of clinical, radiographic, pathologic, and biochemical tools. The most important thing is early and accurate...
Case Report
3 Cases of Congenital Adrenal Hyperplasia.
Kyo Sun Kim, Dong Soo Kim, Seoung Ku Kim, Kwang Ho Kim, Duk Hi Kim, Duk Jin Yun
Clin Exp Pediatr. 1980;23(8):662-669.   Published online August 15, 1980
We present 3 cases of congenital hyperplasia. Case lis a 5 year and 9 month old who is suffered from excessive salt craving and symptoms of precocious puberty. Case llis a 2 month old boy who has failure to thrive and frequent episode of dehydration. Case lll is a 5 year and 3 month old girl who has enlarged clitoris...
Original Article
A Clinical Observation of Congenital Diaphragmatic Hernia.
Kwang Ho Kim, Hun Young Moon, Chang Joon Coe, Duk Jin Yun
Clin Exp Pediatr. 1980;23(7):527-533.   Published online July 15, 1980
Diaphragnatic hernia is one of the surgical emergencies of the childhood because of the life-threatening cardiorespiratory embarrassment frequently associated with it. This congenital condition is characterized by varying degrees of protrusion of the abdominal viscera into the thoracic cavity through an abnormal opening in the diaphragm this opening results from a defect in the complex embryologic developement of the diaphragm...
Clinical Analysis of Congenital Anorectal Malformation.
Kwang Ho Kim, Ki Young Lee, Duk Jin Yin, Eui Ho Hwang
Clin Exp Pediatr. 1980;23(6):438-445.   Published online June 30, 1980
Malformation of the anus and rectum, frequently refered to as imperforate anus are the most common of congenital anomalies among the congenital anomalies of gastrointestinal tract, occuring about once in every 5,000births. They consist of variety of lesions ranging from mild congenital stenosis of the anus which requires simple dilation for cure to complex deformities which present some of the...
Case Report
Histiocytic Medullary Reticulosis: A case record and literatures review.
Kwang Ho Kim, Chi Ok Ahn, Byoung Soo Kim, Kir Young Kim, Dong Wha Lee, In Joon Choi
Clin Exp Pediatr. 1978;21(5):403-411.   Published online May 31, 1978
Histiocytic medullary reticulosis was first described as a clinical and pathological entity by Scott and Robb-Smith in 1939. The clinical pictures include progressive pancytopenia, fever, wasting, lymphadenopathy, hepatosplenomegaly, jaundice and purpura. The outstanding morphological features of the disease is proliferation of histiocytes throughout the reticuloendothelial system with frequent leucoerythrophagocytosis. In spite of uniform clinical and fistologcal pictures verified by additional...
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