1.A Case of Sirenomelia.
Hyun Kuk KIM ; Sung Ik CHO ; Byoung Tae KIM ; Hak Jhoo CHA ; Sang Jhoo LEE
Journal of the Korean Pediatric Society 1990;33(2):241-245
No abstract available.
Ectromelia*
2.Two cases of meconium peritonitis.
Hye Kyung NAM ; Dong Hwan LEE ; Sang Jhoo LEE
Journal of the Korean Pediatric Society 1991;34(2):256-260
No abstract available.
Meconium*
;
Peritonitis*
3.Glucose-6 Phosphate Dehydrogenase Deficiency.
Meen Jai LEE ; Sang Eun LEE ; Dong Whan LEE ; Sang Jhoo LEE ; Sang Chul PARK
Journal of the Korean Pediatric Society 1990;33(2):212-219
No abstract available.
Oxidoreductases*
4.Three Cases of Insulin Dependent Diabetes Mellitus in Children.
Tae Hoon LEE ; Sang Chul PARK ; Chang Hwi KIM ; Sang Man SHIN ; Sang Jhoo LEE
Journal of the Korean Pediatric Society 1983;26(3):285-289
No abstract available.
Child*
;
Diabetes Mellitus*
;
Humans
;
Insulin*
5.A Case of Nonimmunologic Hydrops Fetalis Associated with Down Syndrome.
Sang Eun LEE ; Meen Jai LEE ; Dong Hwan LEE ; Sang Jhoo LEE
Journal of the Korean Pediatric Society 1990;33(2):205-211
No abstract available.
Down Syndrome*
;
Edema*
;
Hydrops Fetalis*
6.A Case of Sjogren-Larsson Syndrome.
Kil Joon LEE ; Jong Bock KIM ; Dong Hwan LEE ; Sang Man SHIN ; Sang Jhoo LEE
Journal of the Korean Pediatric Society 1994;37(12):1757-1761
Sjogren-Larsson Syndrome is a rare disorder chracterized by congenital icthyosis, spastic diplegia or tetraplegia and mental retardation. The inheritance is autosomal recessive, due to deficiency of alcohol dehydrogenase activity of fatty acid matabolism. We have experienced a case of Sjogren-Larsson Syndrome in a 16 month-old male children who have dried thick skin, developmental delay, and spastic diplegia. He also has glistening spot on macula area with irregular high voltage slow wave (2-3Hz) on electroencephalography. From Biopsy finding, Lamella ictyosis with acanthosis and hyperkeratosis in epithelium is shown. He was much improved clinically for skin lesion and developmental status with etretinate supplement. We report the case with brief review of related literatures.
Acitretin
;
Alcohol Dehydrogenase
;
Biopsy
;
Cerebral Palsy
;
Child
;
Electroencephalography
;
Epithelium
;
Etretinate
;
Humans
;
Infant
;
Intellectual Disability
;
Male
;
Quadriplegia
;
Sjogren-Larsson Syndrome*
;
Skin
;
Wills
7.A Case of Congenital Adrenal Agenesis.
Kyeong Wha LEE ; Hyung Jin CHOI ; Sang Man SHIN ; Sang Jhoo LEE ; Dong Wha LEE
Journal of the Korean Pediatric Society 1984;27(11):1118-1122
No abstract available.
8.A Study on Lighting in school.
Kyung Hwan OH ; Woo Ryung LEE ; Sang Cheol PARK ; Dong Hwan LEE ; Sang Jhoo LEE
Journal of the Korean Pediatric Society 1990;33(12):1623-1630
No abstract available.
Humans
9.A study of serologically confirmed measles.
Sang Mook CHOI ; Chang Soo OH ; Sang Chul PARK ; Chang Hwi KIM ; Sang Jhoo LEE
Journal of the Korean Pediatric Society 1992;35(4):508-514
No abstract available.
Measles*
10.Ultrasonographic measurement of the neonatal adrenal glands.
Hae Kyung LEE ; Jae Ock PARK ; Chang Hwi KIM ; Sang Man SHIN ; Sang Jhoo LEE
Journal of the Korean Pediatric Society 1993;36(8):1101-1106
TO determine the normal neonatal adrenal gland size, ultrasonographic examinations were performed in 145 newborn infants. They were divided into 3 groups according to the days of age. The group I is 1~3 days, group II is 6~9 days and group III is 21~50 days of age. 1) The adrenal gland size was as follows. In group I, the length was 29.05mm and the width was 4.02mm. In group II, the length was 24.04mm and the width was 2.79mm. In group III, the length was 19.54mm and the width was 2.21mm. 2) With increasing age, the size of adrenal gland became smaller. 3) The size of adrenal gland correlated well with the birth weight and height. We conclude that the ultrasonographic examination is useful in infant adrenal gland disease.
Adrenal Gland Diseases
;
Adrenal Glands*
;
Birth Weight
;
Humans
;
Infant
;
Infant, Newborn