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Original Article
A case of Beckwith-Wiedemann Syndrome.
Jin Soo Choi, Byung Hee Kim, Young Soo Chon, Hwa Il Kwang, Young Youn Choi, Tai Ju Hwang
Clin Exp Pediatr. 1990;33(3):367-372.   Published online March 31, 1990
The Beckwith-Wiedemann syndrome (exomphalos-macroglossia-gigantism: E M G Syndrome) is characterized by the presence of a wide variety of anomalies such as omphalocele, muscular macroglossia, gigantism, neonatal hypoglycemia, cytomegaly of the adrenal fetal cortex, hyperplasia of gonadal interstitial cells, and hyperplastic visceromegaly, particularly of pancreas and kidneys. Other abnormalities may include hemihypertrophy, microcephaly and mental retardation, prominent occiput, facial flame nevus, neonatal polycythemia, and linear indentations...
Case Report
A Case of Beckwith-Wiedemann Syndrome.
Hyo Sook Hong, Hong Chul Lee, Oh Kyung Lee, Myung Ho Lee
Clin Exp Pediatr. 1987;30(10):1166-1169.   Published online October 31, 1987
Beckwith-Wiedemann syndrome constitutes a clinicopathologic entity characterized macroglossia, omphalocele or umblical hernia, visceromegaly, postnatal gigantism, microcephaly, Nevus flammeus, ear lobe grooves, hemihypertrophy and other abnormalities. The anomalies of the syndrome are facultative and not obligatory. We experience one case of Beck with-Wiedemann syndrome. This 1-day-aged female neonate showed macroglossia, gigantism, omphalocele and hypoglycemia. Review of literature was done briefly.
Original Article
A Clinical Analsys on 39 Cases of Omphalocele and Gastroschisis.
Min Suk Hyun, Mee Yeon Park, Jheong Hee Hahn, So Won Ahn, Jung Woo Yang
Clin Exp Pediatr. 1983;26(9):857-865.   Published online September 30, 1983
A clinical study was done on 39 patients, 21 with omphalocele and 18 with gastroschisis, born at II Sin Women’s Hospital between Jan. 1976 and Dec. 1982. The following results were obtained. 1) In omphalocele 57.1% of the affected babies were males this being slightly higher than the 5.8% in overall distribution of total deliveries but in gastroschisis a reverse of the normal distribution was...
Case Report
A Case of Omphalocele Associated with Multiple Congenital Anomalies.
Yoon Ja Kim, Soo Kyung Jeong, Nam Ji Cho, Jae Keum Ji
Clin Exp Pediatr. 1983;26(1):66-70.   Published online January 31, 1983
A omphalocele associated with multiple congenital anomalies is extremely rare congenital malformation. We experienced a ruptured large omphalocele of short duration associated with multiple congenital anomalies such as patent omphalomesenteric duct, cleft palate and lip, postaxial polydactylia with dystrophic nails on both hands and leftfoot, adrenal heterotophia in left peritesticular region, pancreatic heterotophia in perisplenic lymphnode, nodular excrescene of spleen, and...
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