1.The experience of treacher collins syndrome.
Byeong Woog CHOI ; Kyu Nam PARK ; Ji Woon HA
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1993;20(6):1327-1335
No abstract available.
Mandibulofacial Dysostosis*
2.Surgical correction of congenital ear cartilage deformity using inverted mattress suture.
Byeong Woog CHOI ; In Suck SUH ; Ji Woon HA
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1993;20(1):73-82
No abstract available.
Congenital Abnormalities*
;
Ear Cartilage*
;
Ear*
;
Sutures*
3.Perinatal Prognosis of Single Umbilical Artery.
Yoon Ha KIM ; Tae Bok SONG ; Ji Soo BYUN ; Young Youn CHOI ; Ji Young LEE
Korean Journal of Perinatology 1999;10(2):155-160
OBJECTIVE: To evaluate the perinatal prognosis of fetuses with a single umbilical artery. METHODS: From 1992 to 1998, nineteen cases with single umbilical artery(SUA) was observed in 8,704 deliveries at Chonnam University Hospital. RESULTS: Out of nineteen fetuses, thirteen fetuses with single umbilical artery were detected by antenatal ultrasonographic examination and six fetuses were detected after birth. The male to female ratio was 0.9: 1. Congenital malformations were observed in 8 babies(42.1%) and included leg deformity, esophageal atresia, imperforated anus, ventriculomegaly, meningocele, hydronephrosis, ventricular septal defect, joint contracture, cleft lip and palate, toe anomaly, imperforated anus, kyphosis, no urethra and testis, clubfoot, patent ductus arteriosus and rnild mitral regurgitation. Among 10 cases of karyotyping analysis three cases were diagnosed as trisomy 18. Fourteen fetuses(77.8%) showed growth restriction at delivery. Antenatal obstetric complications were hydramnios(n = 3), oligohydramnios(n =2), and severe preeclampsia(n = 3). CONCLUSION: Careful ultrasonographic evaluation for the identification of a SUA is necessary because of its frequent association with congenital anomaly, growth restriction and cytogenetic abnormality.
Anal Canal
;
Chromosome Aberrations
;
Cleft Lip
;
Clubfoot
;
Congenital Abnormalities
;
Contracture
;
Ductus Arteriosus, Patent
;
Esophageal Atresia
;
Female
;
Fetus
;
Heart Septal Defects, Ventricular
;
Humans
;
Hydronephrosis
;
Jeollanam-do
;
Joints
;
Karyotyping
;
Kyphosis
;
Leg
;
Male
;
Meningocele
;
Mitral Valve Insufficiency
;
Palate
;
Parturition
;
Prognosis*
;
Single Umbilical Artery*
;
Testis
;
Toes
;
Trisomy
;
Urethra
4.Suspectd Malignant Hyperthermia Following Spinal Anesthesia.
Han Soo HA ; Ji Bong HA ; In Chan CHOI ; Yeong Cheol PARK
Korean Journal of Anesthesiology 1994;27(10):1497-1502
Malignant hyperthermia is a metabolic and genetic disease which present with multiple signs of variable intensity and time course. Most of signs are nonspecific to malignant hyperthermia an4 it is not unusual for malignant hyperthermia-susceptible patients to under- go their first anesthesia uneventfully. Thus,the accurate prediction of preanesthetic susceptibility and early diagnosis of malignant hyperthermis can be lifesaving. Recently, some episodes of signs and symptoms suggestive of malignant hyperthemia after spinal an- esthesia those were suspected to be malignant hyperthermia have been reported. In our hospital, two patients suffered from signs and symptoms suggestive of malignant hyperthermia after spinal anesthesia. One patient showed severe muscle rigidity on the un- blocked upper extremities and thorax, tachycardia (120-160beat/min) and hypertension (180-160/120-100mmHg) and later he showed high fever(38-40degrees C), generalized seizure and severe acidosis. He expired the next day of operation in spite of intensive care. The other patient showed shivering, high fever(39degrees C) and elevated serum CPK level(more than 1,500IU/ L) after spinal anesthesia. Intensive treatment with cooling was immediately initiated. Then, he recovered completely 6 hours later. His mother and a brother showed increased serum CPK level(91,112IU/L, respectively), too. Although we could not performed confirmatory diagnostic test, signs and symptoms were very similar to those of malignant hyperthermia. So, we suspected that it might be malignant hyperthermia.
Acidosis
;
Anesthesia
;
Anesthesia, Spinal*
;
Diagnostic Tests, Routine
;
Early Diagnosis
;
Humans
;
Hypertension
;
Critical Care
;
Malignant Hyperthermia*
;
Mothers
;
Muscle Rigidity
;
Seizures
;
Shivering
;
Siblings
;
Tachycardia
;
Thorax
;
Upper Extremity
5.Two cases of angioedema due to C1 inactivator deficiency.
Ji Young SUH ; Jae Kyung CHOI ; Ha Baik LEE ; Chan Keum PARK
Pediatric Allergy and Respiratory Disease 1993;3(1):121-127
No abstract available.
Angioedema*
6.Tinea Manuum Caused by Trichophyton mentagrophytes var. erinacei.
Myung Hoon LEE ; Ji Young YOO ; Moo Kyu SUH ; Gyoung Yim HA ; Jong Soo CHOI
Korean Journal of Dermatology 2012;50(11):1010-1012
No abstract available.
Hedgehogs
;
Tinea
;
Trichophyton
7.A Case of Werdnig-Hoffmann Disease.
Ok Ji HWANG ; Kon Hee LEE ; Ha Joo CHOI ; Woo Kap CHUNG
Journal of the Korean Pediatric Society 1989;32(2):289-296
No abstract available.
Spinal Muscular Atrophies of Childhood*
8.A Case of Werdnig-Hoffmann Disease.
Ok Ji HWANG ; Kon Hee LEE ; Ha Joo CHOI ; Woo Kap CHUNG
Journal of the Korean Pediatric Society 1989;32(2):289-296
No abstract available.
Spinal Muscular Atrophies of Childhood*
9.A Case of Human Tail.
Kon Hee LEE ; Ok Ji HWANG ; Ha Joo CHOI ; Woo Kap CHUNG
Journal of the Korean Pediatric Society 1989;32(2):285-288
No abstract available.
Humans*
10.A Case of Human Tail.
Kon Hee LEE ; Ok Ji HWANG ; Ha Joo CHOI ; Woo Kap CHUNG
Journal of the Korean Pediatric Society 1989;32(2):285-288
No abstract available.
Humans*