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Original Article
Atypical Presentation of Acute Glomerulonephritis
Hyun Ho Shin, Thy Hyung Park, Sung Ho Cha, Byoung Soo Cho, Chang Il Ahn, Young Tae Ko, Moon Ho Yang
Clin Exp Pediatr. 1993;36(7):987-993.   Published online July 15, 1993
Form March 1982 to December 1991, 110 cases of typical post-streptococcal glomerulonephritis and 25 cases of Atypical acute glomerulonephritis were clinically investigated at Department of pediatrics, Kyung Hee University Hospital, and follwing Data were obtained. 1) Male to Femal ratio was 1.8:1 (Atypical AGN). Peak incidence was from 7 to 12 years. 2) The most common preceding infections were upper respiratory infection,...
Hypercalciuria Associated with Nephropathy (diagnosis by renal biopsy)
Hyun Ho Shin, Jae Yoon Kim, Chong Woo Bae, Sung Ho Cho, Byoung Soo Cho, Chang Il Ahn, Young Tae Ko, Moon Ho Yang
Clin Exp Pediatr. 1992;35(11):1509-1513.   Published online November 15, 1992
Idiopathic hypercalciuria is defined as excessive urinary excretion of calcium in normocalcemia without any primary cause. We performed the sono-guided percutaneous renal biopsy for patients of recurrent hematuria, persistent microscopic hematuria, proteinuria and RBC cast to evaluate underlying nephropathy. We could obtained the following results 1) The age at the renal biopsy ranged from 3 years to 14 years. Sex ratio is 1.9:1...
A case of lipodystrophia centrifugalis abdominalis infantilis.
Kyu Young Lee, Sung Ho Cha, Byoung Soo Cho, Chang Il Ahn, Woo Young Sim, Choong Rim Haw, Moon Ho Yang
Clin Exp Pediatr. 1991;34(10):1452-1457.   Published online October 31, 1991
We report a case of lipodystrophia centrifugalis abdominalis infantilis in 24 month male. At age 18 months, his mother noticed a fairly well-defined depression of skin in the both inguinal and axillary area, which gradually spread centrifugally to the lower portion of abdomen and total inguinal and axillary region. The laboratory findings were unremarkable. Biopsy showed absense of subcutaneous fat in the affected area.
3 Cases of Prune Belly syndrome.
Chong Sung Chung, Chong Woo Bae, Byung Soo Cho, Chang Il Ahn, Ju Hie Lee, Moon Ho Yang
Clin Exp Pediatr. 1989;32(6):845-851.   Published online June 30, 1989
The prune belly syndrome is a rare congenital anomaly characterized by laxed, wrinkled abdominal wall, cryptorchidism and urinary tract anomalies. But it has wide spectrum of clinical severity, clinical presentation and other anomalies such as pulmonary and skeletal anomalies. We suggested that we should examine the abdominal wall carefully in order to detect mild form (class III) of prune belly syndrome when we...
Case Report
A case of Finnish Type of Congenital Nephrotic Syndrome.
Jeong Sik Min, Yang Kook Shon, Soo Woong Lee, Suk Chul Kang, Yong Koo Park, Moon Ho Yang
Clin Exp Pediatr. 1982;25(2):175-182.   Published online February 28, 1982
The Finnish type of Congenital Nephrotic Syndrome is characterized by large placenta, early manifestation, growth and developmental delay and resistance to treatment. Authors experienced a case of characteristic Finnish type of Congenital Nephrotic Syndrome in a girl, who was admitted to the Pediatric Department of KHUH at 2 1/1 months of age because of generalized edema and abdominal distension and...
4 Cases of Duchenne type of Progressive Muscular Dystrophy.
Soon Kon Chai, Sang Ho Ko, Soo Woong Lee, Moon Ho Yang
Clin Exp Pediatr. 1979;22(8):729-736.   Published online August 15, 1979
4 cases of Duchenne type of Muscular Dystrophy have been experienced in brothers of 6 years old boy, 8 years old boy whose limb girdle was involved, brothers of 9 years old boy and other brothers of 9 years old boy. Ina all cases, serum CPK levels were significantly increased and typical waddling gait and Gower's sigh were noticed. The...
Original Article
Four Cases of Anencephaly with Multiple Anomalies.
Sang Ho Ko, Whi Dai Kim, Soo Woong Lee, Sang Man Shin, Chang Il Ahn, Jung Eun Mok, Moon Ho Yang
Clin Exp Pediatr. 1977;20(8):633-638.   Published online August 31, 1977
The incidence of anencephaly ranges from 0.1 to 6.7 per 1,000 births. Female fetuses predominated, especially among prematures, with a ratio of between 3 and 7 to 1. The infants are either stillborn or die within a few days of birth. By about 23 days?gestational age the neural tube is complete, except for an opening at each end, the anterior...
Case Report
A Case of Cushing’s Syndrome
Sang Ho Ko, Soo Ha Park, Sang Man Shin, Joong Sik Kim, Choong Yoon, Moon Ho Yang
Clin Exp Pediatr. 1975;18(11):848-855.   Published online November 30, 1975
A case of Cushing’s syndrome in 10-year-old girl is presented who was admitted to the Pediatric ward of Kyung Hee University Hospital with the complaints of moon face, obesity and hirsutism. The diagnosis was confirmed by characteristic clinical features, biochemical studies, radiological studies and pathologic examination. The tumor was removed successfully and final diagnosis was adrenocortical carcinoma of the Rt....
Original Article
A Case of Cryptococcosis Associated with Eosinophilia
Chang Hwi Kim, Whi Dai Kim, Sang Man Shin, Joong Sik Kim, Moon Ho Yang, Jae Doo Ahn
Clin Exp Pediatr. 1975;18(7):511-517.   Published online July 31, 1975
Authors experienced a case of Cryptococcosis accompanied by eosinophilia in a 12 years 8 months old Korean boy. He was admitted to our hospital due to high fever and intermittent coughing. Lymphnode biopsy showed Cryptococcus neoformans, which was obtained at left inguinal region. And tlie organism was found on the culture of cerebrospinal fluid. Brief review of related literature were presented.
Two Cases of Duchenne Type of Muscular Dystrophy in Sisters
Soo Ha Park, Eui Hyun Jo, Sang Man Shin, Sang Jhoo Lee, Moon Ho Yang
Clin Exp Pediatr. 1974;17(9):607-612.   Published online September 30, 1974
Authors has experienced two cases of Duchenne type of muscular dystrophy in 8 years old female child and in her 2 years old sister. Initial symptoms were frequent fall and waddling gait in these two cases which has began to develop at the age of 4 years in elder sister and at the age of 2 years in younger sister. Diagnosis has confirmed by...
Case Report
An Autopsy Case of Congenital Jejunal Atresia
Soo Ha Park, Sang Man Shin, Sang Jhoo Lee, In Keun Bae, Hoong Zae Joo, Moon Ho Yang
Clin Exp Pediatr. 1974;17(2):144-148.   Published online February 28, 1974
This is an autopsy case of congenital jejunal atresia in an 11-hour-old male newborn infant who was admitted to pediatric ward because of bile stained vomitus, abdominal distention and no passage of meconium stools. End to side jejunioleostomy has carried out on 2nd hospital day and expired on 6th hospital day. The site of atresia was in distal portion of the jejunum which was...