- Case Report
- A Case of Sturge-Weber Syndrome.
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Jin Soo Jo, Moon Chung Cho, Doo Seong Moon, Kyung Sook Cho, Chong Dae Cho
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Clin Exp Pediatr. 1986;29(4):451-456. Published online April 30, 1986
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- A Case of Sirenomelia.
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Moon Chung Chao, Sae Jin Lee, Jin Soo Jo, Hyun Sook Kim, Doon Seong Moon, Chong Dae Cho
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Clin Exp Pediatr. 1986;29(3):332-335. Published online March 31, 1986
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A l,500gm undetermined sex neonate was born after 30 weeks gestation to a 26 years old primipara mother.
On physical examination, he was noticed massive abnormality of the lower half of the body with absence of the anus and external genitalia and fusion of the lower extremities throughout their length.
We confirmed this case by physical examination and x-ray study. A brief... |
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- A Case of Congenital Hypoplastic Anemia.
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Sae Jin Lee, Moon Chung Cho, Kyung Sook Cho, Doo Sung Moon, Chong Dae Cho
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Clin Exp Pediatr. 1985;28(8):801-804. Published online August 31, 1985
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We observed a case of congenital hypoplastic anemia in a 10 month old male patient who was diagnosed through bone marrow aspiration. This steroid-unresponsive patient has been maintaining a concentration of hemoglobin
compatible with health from supportive transfusion therapy. A brief review of related literature was made.
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- A Case of Tuberous Sclerosis.
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Ju Kyeong Lee, Kwang Soo Hwang, Kyung Sook Cho, Doo Sung Moon, Chong Dae Cho
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Clin Exp Pediatr. 1985;28(5):514-517. Published online May 31, 1985
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We experienced a case of tuberous sclerosis diagnosed by typical clinical manifestations and brain CAT in a 3 year 5 month old girl. We presented the case with the brief review of the literatures.
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- Original Article
- Hepatobiliary Scintigraphy with 99mTc-DISIDA in the Evaluation of Neonatal Jaundice.
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Kwang Soo Hwang, Sae Jin Lee, Kyung Sook Cho, Chong Dae Cho, Bok Hwan Park
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Clin Exp Pediatr. 1984;27(7):664-672. Published online July 31, 1984
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Hepatobiliary scintigraphy with 99mTc-DISIDA was used to evaluate neonates with direct hyperbilirubinemia who were admitted to the department of Pediatrics, Maryknoll hospital, between May 1981 and Jun. 1983.
1)Total number of patients were 10, boys to girls ratio was 4:1, and age distribution ranging from 9 to 200 days of age. 2)Initial studies of the seven patients intrahepatic cholestasis showed definite... |
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- Case Report
- A Case of Thanatophoric Dwarfism.
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Young Kyun Hwang, Soo Baeck LEE, Chong Dae Cho, Ju Kyeong Lee, Doo Seong Moon
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Clin Exp Pediatr. 1983;26(11):1129-1132. Published online November 30, 1983
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We experienced a case of Thanatophoric dwarfism.
A 1870 gm male neonate was born after 31 weeks gestation to a 33 years old gravida 1mother
with polyhydramnios. On physical examination, he was noticed micromelic dwarfism, narrow thorax,
and saddle nose. We confirmed this case by physical examination and X-ray study.
A brief review of literatures were presented.
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- A Case of SprengeVs Deformity
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Chong Dae Cho, Hyo In Bae
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Clin Exp Pediatr. 1968;11(4):193-196. Published online April 30, 1968
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A case of SprengeFs deformity in a 5 year-old male orphan is presented. He was admitted to Pusan Children’s Charity Hospital in July, 1967, because of moderately limitted elevation and abduction of his left arm and abnormally elevated his left scapula. On physical examination, he was normally developed and moderately nourished, but asymmertrically his lift scapula was 2 cm higher... |
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- A Case of Embryonal Carcinoma of the Testis with Metastasis in the Lung
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Jang Jae Cho, Chong Dae Cho
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Clin Exp Pediatr. 1968;11(4):197-200. Published online April 30, 1968
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A case of embryonal carcinoma of the testis in a 2 year-1 month old child, metastatized to both lungs, is reported.
Pathological picture are as follows: There are new foci composed of neoplastic cells, which reveals considerable cellular and architectural variation. The tumor is| made up of closed packed, large, highly anaplastic epitherial type of cells with ampholic cytoplasm without definite... |
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- A Case of Amyotrophic Lateral Sclerosis
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Sae Joon Choe, Chong Dae Cho, Hyo In Bae, Dong Gwon Kim
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Clin Exp Pediatr. 1967;10(7):381-384. Published online July 31, 1967
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The authors experienced a child of amyotrophic lateral sclerosis that is extremely rare in childhood but mainly seen in the middle-aged, and report with review of literatures.
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