- Original Article
- Surfactant replacement therapy in neonatal respiratory distress syndrome.
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Chan Ok Park, Boung Yul Lim, Byeong Gie Yeo, Ji Ho Song, Eun Kyung Sohn, Chong Woo Bae, Sa Jun Chung, Chang Il Ahn
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Clin Exp Pediatr. 1991;34(9):1211-1222. Published online September 30, 1991
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Respiratory distress syndrome (RDS) in tiny infants remains a major medical challenge as they are
less tolerant of supportive care.
In 1959, after identification of the pulmonary surfactant (S), S replacement therapy were used to
treat RDS. This idea was first successfully tested on RDS infants by Fujiwara, et. al” in 1980. Now
the trial and use of S for the treatment in RDS... |
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- Accuracy of anorectal manometry in the diagnosis of congenital megacolon.
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Jong Yul Jeon, Byeong Gie Yeo, Chong Woo Bae, Yong Mook Choi, Chang Il Ahn, Young Woon Chang
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Clin Exp Pediatr. 1991;34(5):614-620. Published online May 31, 1991
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Thirty-seven patients with clinical impression of congenital megacolon were studied with anorectal
manometry for the evaluation of its diagnostic accuracy. Including 12 neonates, their age ranged form
3 days to 8 years and barium enema was performed to all of them except one. The results of
rectosphincteric reflex (RSR) of anorectal manometry was compared with the final diagnosis, which
was obtained by clinical course,... |
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- A Case of (21q 21q) Translocation Down Syndrome Inherited from a t(21q 21q) Balanced Carrier Mother.
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Byeong Gie Yeo, Chong Woo Bae, Yong Mook Choi, Chang Il Ahn, Bo Hoon Oh
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Clin Exp Pediatr. 1990;33(7):1004-1008. Published online July 31, 1990
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Vast majority of t(21q 21q) Down syndrome occur de novo and familial cases are extremely rare.
In familial translocation Down syndrome, One of the parent show 45 chromosomes.
In general, the carrier parent carrying (21q 21q) translocation is phenotypically normal because
significant amount of genetic material has not been lost in the translocation process. Homologous
Robertsonian translocation can be produced either by abnormal gametogenesis... |
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