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Case Report
A Case of Moyamoya Disease with Neurofibromatosis Type I
Mi A Lee, Joo Pil Eum, Hae Young Lee, Byung Ho Cha
Clin Exp Pediatr. 2005;48(1):93-96.   Published online January 15, 2005
Neurofibromatosis type I is an autosomal dominant disorder with varied manifestations in bone, soft tissue, the nervous system and skin. This is characterized by cafe-au-lait spots, neurofibromas, Lisch nodules, optic glioma, bony displasia, and intertriginous freckling. One of the more serious aspect of the disease relates to the arterial involvement. Vascular changes in neurofibromatosis may occur in any arterial tree...
The VACTERL Association : Tracheal Stenosis, Tracheal Bronchus and Partial Pulmonary Agenesis, Instead of Tracheoesophageal Fistula
Ji Sook Park, Hae Young Lee, Jong Sil Lee, Ji Hyeon Seo, Jae Young Lim, Myong Bum Choi, Chan Hoo Park, Hyang Ok Woo, Hee Sang Youn
Clin Exp Pediatr. 2004;47(10):1119-1123.   Published online October 15, 2004
VACTERL association is a disease with multiple congenital anomalies of the vertebrae, anus, cardia, tracheoesophageal(TE) fistula, renal and limb. This disease is derived from VATER anomaly, accompanied by cardiac and limb anomalies. We experienced a case of a 1-day-old boy with anal atresia, who represented multiple anomalies during hospital course. The multiple anomalies were hemivertebra, anal atresia, complex heart disease(coarctation...
Original Article
A case of double compartment hydrocephalus.
Eun Kyung Oh, Hae Young Lee, Jae Seung Yang, Chul Hu, Young Hyuk Lee
Clin Exp Pediatr. 1991;34(9):1305-1310.   Published online September 30, 1991
The double compartment hydrocephalus is now recognized as a clinical entity needing early diagnosis and treatment. By definition, the concept of double compartment hydrocephalus indicates seperate and individually progressing, usually sequential, hydrocephalus of the supratentorial and infratentorial CSF ventricles. In most instances, this entity consists of supratentorial hydrocephalus of the third and lateral ventricles (as a result of aqueductal stenosis) that has been treated...
A Case of Hypertrophic Cardiomyopathy in Identical Twin.
Wea Kyoung Shin, Hae Young Lee, Hwang Min Kim, Jae Seung Yang, Baek Keun Lim, Jone Soo Kim
Clin Exp Pediatr. 1990;33(10):1399-1405.   Published online October 31, 1990
Hypertrophic cardiomyopathy is a common genetically transmitted disorder characterized by asymmetric septal hypertrophy and systolic anterior motion of the mitral valve. We have recently experienced identical twin with the hypertrophic cardiomyopathy confirmed by M-mode and 2-D echocardiography. It is the first report of hypertrophic cardiomyopathy in identical twin in Korea. So presented this case with a review of referential literatures.
The Relationship of Specific Gravity by Refractometer and Osmolality in the Urine of Neonates.
Hae Young Lee, In Soon Ahn, Jae Seung Yang, Beak Keun Lim, Jong Soo Kim
Clin Exp Pediatr. 1988;31(5):555-558.   Published online May 31, 1988
Comparison of urinary specific gravity by refractometer and osmolality in 238 neonates demonstrated as followings; 1) The regression line is represented by the equation: Y = 107+14.2 (X-1000) while Y = osmolality in mosm/kg X = Specific gravity by refractometer r=0.8545 2) Osmolality is the only accurate measure of urine concentration in newborn infants. If the specific gravity by refractometer is used to screen for urine concentration, an elevated level...
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