1.A Clinical Observation of Congenital Anomalies Born with Hydramnios.
Kook In PARK ; Myung Shik LEE ; Chul LEE ; Dong Gwan HAN
Journal of the Korean Pediatric Society 1984;27(10):991-999
No abstract available.
Polyhydramnios*
2.A Case of Large Placental Chorioangioma Combined with Polyhydramnios.
Ho Hyoung LEE ; Jong Dae KIM ; Eun Cheol JANG ; Eun Sik SOHN ; Hee Taek LIM ; Chun Bo LEE ; Seung Kwan SHIN
Korean Journal of Obstetrics and Gynecology 2000;43(9):1652-1655
No abstract available.
Hemangioma*
;
Polyhydramnios*
3.Indomethacin therapy in polyhydramnios : a case report.
Soon Ha YANG ; Ji Hee LEE ; Mee Lee LEE ; Eun Hwan JEONG ; Bo Hyun YOON ; Hee Chul SYN ; Syng Wook KIM
Korean Journal of Perinatology 1993;4(3):422-427
No abstract available.
Indomethacin*
;
Polyhydramnios*
4.Clinical study on 44 cases of infant born to polyhydramniotic mother.
Byung Min MOON ; Chun Ho CHO ; Kyoung Sim KIM ; Ki Bok KIM
Journal of the Korean Pediatric Society 1992;35(5):630-638
No abstract available.
Humans
;
Infant*
;
Mothers*
;
Polyhydramnios
5.The Cause, Diagnosis, and Management of Polyhydramnios.
Korean Journal of Perinatology 2012;23(2):50-60
Amniotic fluid plays an important role in fetal development and growth. Amniotic fluid volume should be maintained adequately throughout gestational periods. Polyhydramnios is a relatively common obstetrical problem, but is associated with poor perinatal outcome both in mother and fetus. For the proper management of polyhydramnios, it is important to find out accurate causes, but it is not easy even if obstetricians perform thorough prenatal assessments. It is also important to understand the regulation of amniotic fluid volume. Based on these backgrounds, this article will briefly review mechanisms of the regulation of amniotic fluid, and will also review diagnosis, etiologies, managements and prognosis of polyhydramnios.
Amniotic Fluid
;
Female
;
Fetal Development
;
Fetus
;
Humans
;
Mothers
;
Polyhydramnios
;
Prognosis
6.A Case of Pena-Shokeir Phenotype in Trisomy 18 Syndrome.
Ki Hun SONG ; Jee Yeon SONG ; In Kyung SUNG ; Kyong Su LEE
Journal of the Korean Pediatric Society 1997;40(9):1303-1308
Pena-Shokeir syndrome is a rare, often lethal disease, characterized by intrauterine growth retardation, craniofacial anomalies, limb ankylosis, polyhydramnios and pulmonary hypoplasia. This autosomal recessive disease should be differentiated from trisomy 18, which the second most common multiple congenital malformation syndrome. It is therefore clear that the two syndromes have certain features in common, the most consistent being craniofacial and limb abnormalities and intrathoracic pathology. Therefore, final diagnosis should be based on chromosome study. The case that we experienced had typical Pena-Shokeir phenotype, but chromosomal study show 47, XY, +18.
Ankylosis
;
Diagnosis
;
Extremities
;
Fetal Growth Retardation
;
Pathology
;
Phenotype*
;
Polyhydramnios
;
Trisomy*
7.A Case of Esophageal Atresia Associated with Malrotation and Segemental Dilatation of the Ileum.
Jung Il PARK ; In Kyu LEE ; Young Tack SONG
Journal of the Korean Surgical Society 2000;59(1):124-127
A case of esophageal atresia associated with malrotation and segmental dilatation of the ileum is described. To our knowledge, this is the first such report of this combination of features. The prenatal sonogram showed polyhydramnios. Esophageal atresia was diagnosed 3 days after birth. The diagnosis of malrotation and segmental dilatation of the ileum was made using a barium enema and an explolaparotomy 10 days after the first operation. The facts indicate that abnormal findings on a prenatal sonography and esophageal atresia may be associated with many congenital anomalies should be considered.
Barium
;
Diagnosis
;
Dilatation*
;
Enema
;
Esophageal Atresia*
;
Ileum*
;
Parturition
;
Polyhydramnios
8.A Case of Acardiac Twin.
Hak Youle PARK ; Jun Young SEO ; June Baek SONG ; Tae Sang KIM ; Ik Soo KIM
Korean Journal of Obstetrics and Gynecology 1999;42(10):2371-2376
Acardiac twinning affects 1 in 100 monozygotic twin pregnancies and 1 in 35,000 pregnancies overall. This condition is characterized by the absence or rudimentary development of fetal heart, and associated with various anomaly. The presence of an acardiac twin requires the normal (or "pump") twin to provide circulation for itself, as well as the acardiac sibling. The acardiac malformations are uniformly fatal in the affected twin, and mortality in the co-twin is as high as 55%. The principal perinatal problems associated with acardiac twinning are pump-twin congestive heart failure, maternal hydramnios, and preterm delivery. We recently experienced a case of acardius anceps associated with a normal male infant, so present with a brief review of the literature.
Fetal Heart
;
Heart Failure
;
Humans
;
Infant
;
Male
;
Mortality
;
Polyhydramnios
;
Pregnancy
;
Siblings
;
Twins, Monozygotic
9.A Case of Nonimmune Hydrops Fetalis due to Placental Chorioangioma.
Jun Hyeon KIM ; In Jeong KIM ; In Seok KIM ; Jin Soo CHOI ; Woo Gill JEONG
Journal of the Korean Pediatric Society 1997;40(1):124-128
Fetal hydrops describes the infant who has generalized edema due to accumulation of exess fluid, in serious case, ascites and pleural and pericardial effusions are commonly combined. The chorioangioma is considered the most common primary tumor of the placenta, which is about 1% of all pregnancy. However, the majority of the cases are asymptomatic but larger ones, usually more than 5cm in diameter, are commonly associated with maternal and fetal complications. We report a case of nonimmune hydrops fetalis due to large chorioangioma with associated polyhydramnios. The newborn infant was managed conservatively and had excellent outcome.
Ascites
;
Edema
;
Hemangioma*
;
Humans
;
Hydrops Fetalis*
;
Infant
;
Infant, Newborn
;
Pericardial Effusion
;
Placenta
;
Polyhydramnios
;
Pregnancy
10.A Case of Nonimmune Hydrops Fetalis due to Placental Chorioangioma.
Jun Hyeon KIM ; In Jeong KIM ; In Seok KIM ; Jin Soo CHOI ; Woo Gill JEONG
Journal of the Korean Pediatric Society 1997;40(1):124-128
Fetal hydrops describes the infant who has generalized edema due to accumulation of exess fluid, in serious case, ascites and pleural and pericardial effusions are commonly combined. The chorioangioma is considered the most common primary tumor of the placenta, which is about 1% of all pregnancy. However, the majority of the cases are asymptomatic but larger ones, usually more than 5cm in diameter, are commonly associated with maternal and fetal complications. We report a case of nonimmune hydrops fetalis due to large chorioangioma with associated polyhydramnios. The newborn infant was managed conservatively and had excellent outcome.
Ascites
;
Edema
;
Hemangioma*
;
Humans
;
Hydrops Fetalis*
;
Infant
;
Infant, Newborn
;
Pericardial Effusion
;
Placenta
;
Polyhydramnios
;
Pregnancy