- Case Report
- A Case of Bilateral Vocal Cord Paralysis in Neonate
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Young Kyoun Kim, Seung Cheol Lee, Se Wook Oh, Sang Woo Kim, Jae Hyung Park
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Clin Exp Pediatr. 1998;41(4):558-561. Published online April 15, 1998
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Neonatal vocal cord paralysis is the second most common laryngeal anomaly, which accounts for
approximately 10% of all congenital laryngeal lesions. Neonate with bilateral vocal cord paralysis
are charactenzed with a glottic obstruction which usually shows dyspnea and inspiratory stridor.
Treatment of bilateral vocal cord paralysis in neonate have two major goals : restore proper
breathing and retain the voice. Tracheostomy is the best... |
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- A Case of Genital Prolapse in Premature Baby
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Woong Kyu Choi, Seung Cheol Lee, Yong Won Park, Chong Guk Lee, Sang Woo Kim
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Clin Exp Pediatr. 1998;41(2):281-284. Published online February 15, 1998
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Neonatal genital prolapse is very rare and is usually associated with meningomyelocele or other anomalies of the central nervous system. Synonyms of genital prolapse are sacropubic hernia, pelvic relaxation, and pelvic organ prolapse. There are two types of genital prolapse including vaginal prolapse and uterovaginal prolapse. We experienced a case of uterovaginal prolapse in a 30 day-old premature infant, which... |
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- A Case of Lipoid Pneumonia with Hypercalcemia Caused by SqualelneⓇ Intake by Force
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Young Kyoun Kim, Ho Suk Kang, Seung Cheol Lee, Chong Guk Lee, Sang Woo Kim
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Clin Exp Pediatr. 1997;40(12):1745-1749. Published online December 15, 1997
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Lipoid pneumonia is a chronic, interstitial, proliferative inflammation resulting from aspiration of
lipoid material and occurs principally in debilated infants.
We experienced a case of lipoid pneumonia with hypercalcemia in a 15 month-old boy who showed
irritability, poor weight gain, cough, dyspnea, fatigue, diarrhea and pale face after ingestion of
SqualeneⓇ(shark liver oil : 20-30 cap/day) by force for 2 months.
Calcium preparation was also... |
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- Two Siblings of Non Salt Losing Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
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Seung Cheol Lee, Byung Kyu Suh, Byung Churl Lee
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Clin Exp Pediatr. 1995;38(4):574-581. Published online April 15, 1995
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Congenital adrenal hyperplasia in caused by a defect in the biosynthesis of cortisol as a result of deviciency in one of the essential enzymes, most commonly 21-hydroxylase and is an autosomal recessive disease in close genetic linkage with HLA.
The common clinical manifestations of congenital adrenal hyperplasia is progressive virilization in both sexes, abnormal external genitalia in the... |
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- Original Article
- A Case of Hemolytic Uremic Syndrome.
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Seung Cheol Lee, Chong Guk Lee, Seong Hwan Kim, Sang Woo Kim, Hyun Soon Lee
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Clin Exp Pediatr. 1990;33(8):1140-1147. Published online August 31, 1990
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A female child aged 7 months was admitted because of high fever, vomiting and stuporous
conciousness and revealed to have hemolytic uremic syndrome. Anuria persisted 13 days and required
peritoneal dialysis 4 times a day during the anuric period. Her kidney function recovered somewhat
after dialysis but neurologic complications of marked hydrocephalus and brain atrophy remained. |
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