- Original Article
- Observation on neurocysticercosis in childhood.
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Hae Jung Park, Seong Hee Jang, Se Hee Hwang, Jae Il Sohn, Yong Seung Hwang, Kyu Chang Wang, Byug Kyu Cho, In One Kim, Kyung Mo Yeun, Je Geun Chi, Seung Yull Cho
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Clin Exp Pediatr. 1991;34(6):877-889. Published online June 30, 1991
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A clinical study was performed on 5 patients of neurocysticercosis in childhood who admitted to the Seoul
National University Hospital for the last two years. The conclusions were as follows:
1) Boys were more than girls with the ratio of 4:1. The average age was 9.5.
2) Three out of five lived in Jeju Island. Three had familial history of taeniasis.
3) Three out of five were... |
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- Clinical Observation on Moyamoya Disease in Childhood.
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Se Hee Hwang, Jae Il Sohn, Yong Seung Hwang
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Clin Exp Pediatr. 1990;33(2):178-188. Published online February 28, 1990
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Although the etiology and treatment of moyamoya disease are unknown, the surgical correction is
expected as a good treatment method. But its effectiveness is not confirmed until now. A clinical
study was performed on 21 patients of moyamoya disease in childhood who admitted to the
Pediatric and Neurosurgical department of SNUCH from Jan. 1980 till July 1989.
The results were as follows:
1) The ratio of... |
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- A Clinical Study on Patients with Sydenham's Chorea.
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Jae Il Sohn, Young Sik Kim, Yong Seung Whang
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Clin Exp Pediatr. 1989;32(7):1017-1022. Published online July 31, 1989
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A clinical study was performed on 23 patients of Sydeham’s chorea in the children who admitted
to the pediatric department of SNUH from Jan. 1980 to Dec. 1987.
The results were as follows:
1) Among 316 patients with rheumatic fever, 10 patients (3%) had a chorea.
2) The age at onset of chorea ranged from 8 to 16 years.
3) The ratio of female to male was 1.9... |
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- A Case of Mixed Gonadal Dysgenesis.
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Byung Ran Yun, Jae Il Sohn, Sei Won Yang, Hyung Ro Moon, Je Geun Chi
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Clin Exp Pediatr. 1989;32(12):1757-1762. Published online December 31, 1989
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Mixed gonadal dysenesis is a disorder of sexual differentiation which is characterized by streak
gonad associated with contralateral tesis, persistent Mullerian duct structures and/or sex
chromosomal mosaicism most commonly with 45, X/46, XY.
The authors experienced a case of mixed gonadal dysgensis in a 6-year old child who was reared
as female and admitted due to clitoral enlargement.
The patient had asymmetrical gonads consisted with... |
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