- The Amniotic Fluid Proteome Differs Significantly between Donor and Recipient Fetuses in Pregnancies Complicated by Twin-to-Twin Transfusion Syndrome
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Kim SM, Cho BK, Kim BJ, Lee HY, Norwitz ER, Kang MJ, Lee SM, Park CW, Jun JK, Yi EC, Park JS
- KMID: 2471801
- J Korean Med Sci.
- 2020 Mar;35(10):e73.
- doi: 10.3346/jkms.2020.35.e73
BACKGROUND: Twin-to-twin transfusion syndrome (TTTS) is a serious complication of monochorionic twin pregnancies. It results from disproportionate blood supply to each fetus caused by abnormal vascular anastomosis within the placenta.... -
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- The role of antibiotic prophylaxis in mild to moderate isolated hydronephrosis detected in antenatal screening
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Rianthavorn P, Phithaklimnuwong S
- KMID: 2471076
- Investig Clin Urol.
- 2020 Mar;61(2):200-206.
- doi: 10.4111/icu.2020.61.2.200
PURPOSE: To determine whether continuous antibiotic prophylaxis (CAP) could prevent urinary tract infection (UTI) in mild to moderate antenatal isolated hydronephrosis (IH), characterized by hydronephrosis without ureter and bladder abnormalities,... -
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- Prenatal diagnosis of harlequin ichthyosis: a case report
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Vijayakumari M, Reddy DK, Routhu M, Vuchuru M, Reddy NS
- KMID: 2467937
- Obstet Gynecol Sci.
- 2020 Jan;63(1):94-97.
- doi: 10.5468/ogs.2020.63.1.94
Harlequin ichthyosis (HI) is a rare and severe form of ichthyosis and is characterized by thickened, hard, armor-like plates of skin that cover the entire body. This disease is caused... -
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- Diagnosis of Tuberous Sclerosis Complex and Epilepsy Outcomes in Children with Fetal Cardiac Rhabdomyoma: A Long Term Follow-up Study
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Kim D, Kim HJ, You SJ, Yum MS, Ko TS
- KMID: 2470589
- Ann Child Neurol.
- 2019 Dec;27(4):128-134.
- doi: 10.26815/acn.2019.00185
PURPOSE: Prenatal diagnosis of cardiac rhabdomyoma is suggestive of the presence of tuberous sclerosis complex (TSC), which is commonly associated with epilepsy. This study investigated the diagnostic rate of TSC,... -
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- Fetal Ultrasonography for Prenatal Detection of Tuberous Sclerosis Associated with Cardiac Rhabdomyoma
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Kang MJ, Hong SY, Kwon BY, Jeong JE, Bae JY
- KMID: 2468546
- Perinatology.
- 2019 Dec;30(4):240-243.
- doi: 10.14734/PN.2019.30.4.240
Cardiac rhabdomyoma is common cardiac mass found during the fetal period. Cardiac rhabdomyoma and tuberous sclerosis have significant associations. Tuberous sclerosis in newborns can cause disability in nearly all organs.... -
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- Evaluation of the Early Onset Neonatal Sepsis according to Two Antenatal Group B Streptococcus Screening Methods: Risk-Based versus Universal Screening
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Hong JY, Kim SH, Kim SM, Yee CA, Choi SJ, Oh SY, Roh CR
- KMID: 2468540
- Perinatology.
- 2019 Dec;30(4):200-207.
- doi: 10.14734/PN.2019.30.4.200
OBJECTIVE: The standard antenatal screening method for Group B Streptococcus (GBS) has not been established yet. Therefore, many practitioners in South Korea offer GBS screening to all pregnant women without... -
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- Three Cases of Nasal Chondromesenchymal Hamartoma Occurred in Sinonasal Tract
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Choi Y, Jang YJ, Cho KJ, Chung YS
- KMID: 2466715
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2019 Nov;62(11):651-656.
- doi: 10.3342/kjorl-hns.2018.00815
Nasal chondromesenchymal hamartoma (NCMH) is a rare benign tumor of the sinonasal tract. Most NCMH has a benign nature and can be cured by complete resection. Only a few NCMH... -
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- Pseudo-Single Umbilical Artery by Spontaneous Intrauterine Umbilical Artery Thrombosis
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Baik M, Im SY, Lee G
- KMID: 2460034
- Perinatology.
- 2019 Sep;30(3):183-185.
- doi: 10.14734/PN.2019.30.3.183
Umbilical artery thrombosis is rare event and few prenatally diagnosed cases have been reported. Antenatal diagnosis is very critical, as it is associated with high risk of perinatal motility and... -
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- The Management and Outcomes of Placental Adhesion
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Kim SY, Kong SK, Lee YJ
- KMID: 2453037
- Perinatology.
- 2019 Jun;30(2):47-53.
- doi: 10.14734/PN.2019.30.2.47
Placenta adhesion, often involving placenta accreta, placenta increta, and placenta percreta, is a clinical term used to describe placenta that does not separate spontaneously and cannot be removed without causing... -
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- Clinical Validation of Non-Invasive Prenatal Testing for Fetal Common Aneuploidies in 1,055 Korean Pregnant Women: a Single Center Experience
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Lee DE, Kim H, Park J, Yun T, Park DY, Kim M, Ryu HM
- KMID: 2449987
- J Korean Med Sci.
- 2019 Jun;34(24):e172.
- doi: 10.3346/jkms.2019.34.e172
BACKGROUND: Non-invasive prenatal testing (NIPT) using cell-free fetal DNA from maternal plasma for fetal aneuploidy identification is expanding worldwide. The objective of this study was to evaluate the clinical utility... -
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- The Effect of Multidisciplinary Approach on the Birth Rate of Fetuses with Prenatally Diagnosed Congenital Heart Disease
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Kim ST, Song J, Huh J, Kang IS, Yang JH, Jun TG, Oh SY, Choi SJ, Roh CR
- KMID: 2449985
- J Korean Med Sci.
- 2019 Jun;34(24):e170.
- doi: 10.3346/jkms.2019.34.e170
BACKGROUND: This study aimed to determine the effect of a multidisciplinary approach on the birth rate of fetuses with prenatally diagnosed congenital heart diseases (CHDs). METHODS: Among the fetuses of 724... -
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- Multiple Congenital Pancreatic Cysts in a Neonate
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Kwon EM, Shin J, Jeon GW
- KMID: 2451610
- Neonatal Med.
- 2019 May;26(2):117-120.
- doi: 10.5385/nm.2019.26.2.117
Congenital pancreatic cysts are rare in newborn babies, and this makes prenatal diagnosis difficult. Diagnosis can be delayed for a few months after birth until the infant presents with an... -
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- Recent progress in laboratory diagnosis of thalassemia and hemoglobinopathy: a study by the Korean Red Blood Cell Disorder Working Party of the Korean Society of Hematology
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Lee YK, Kim HJ, Lee K, Park SH, Song SH, Seong MW, Kim M, Han JY
- KMID: 2451051
- Blood Res.
- 2019 Mar;54(1):17-22.
- doi: 10.5045/br.2019.54.1.17
Genetic hemoglobin disorders are caused by mutations and/or deletions in the α-globin or β-globin genes. Thalassemia is caused by quantitative defects and hemoglobinopathies by structural defect of hemoglobin. The incidence... -
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- The Clinical Importance of the Prenatal Diagnosis of Fetal Scalp Hemangioma
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Hwang HS, Koo JH, Kim SY, Kim RY, Wie JH, Ko HS, Park IY, Shin JC
- KMID: 2443173
- Perinatology.
- 2019 Mar;30(1):27-31.
- doi: 10.14734/PN.2019.30.1.27
Scalp hemangioma is a rare disease of the extracranial mass in the fetus. Here, we demonstrate a case of fetal scalp hemangioma as evaluated by prenatal ultrasonography and magnetic resonance... -
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- Prenatal ultrasonography of craniofacial abnormalities
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Mak AS, Leung KY
- KMID: 2433288
- Ultrasonography.
- 2019 Jan;38(1):13-24.
- doi: 10.14366/usg.18031
Craniofacial abnormalities are common. It is important to examine the fetal face and skull Epub ahead of print during prenatal ultrasound examinations because abnormalities of these structures may indicate the... -
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- The clinical usefulness of non-invasive prenatal testing in pregnancies with abnormal ultrasound findings
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Boo H, Kim SY, Seoung ES, Kim MH, Kim MY, Ryu HM, Han YJ, Chung JH
- KMID: 2435946
- J Genet Med.
- 2018 Dec;15(2):79-86.
- doi: 10.5734/JGM.2018.15.2.79
PURPOSE: This study aimed to evaluate the clinical usefulness of non-invasive prenatal testing (NIPT) as an alternative testing of invasive diagnostic testing in pregnancies with ultrasound abnormalities. MATERIALS AND METHODS: This... -
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- Korean physicians' attitudes toward the prenatal screening for fetal aneuploidy and implementation of non-invasive prenatal testing with cell-free fetal DNA
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Kim SH, Kim KW, Han YJ, Lee SM, Lee MY, Shim JY, Cho GJ, Lee JH, Oh SY, Kwon HS, Cha DH, Ryu HM
- KMID: 2435945
- J Genet Med.
- 2018 Dec;15(2):72-78.
- doi: 10.5734/JGM.2018.15.2.72
PURPOSE: Physicians' attitudes may have a strong influence on women's decision regarding prenatal screening options. The aim of this study is to assess the physicians' attitudes toward prenatal screening for... -
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- Prenatal chromosomal microarray analysis of fetus with increased nuchal translucency
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Shim SH, Cha DH
- KMID: 2435942
- J Genet Med.
- 2018 Dec;15(2):49-54.
- doi: 10.5734/JGM.2018.15.2.49
Nuchal translucency is an important indicator of an aneuploid fetus in prenatal diagnostics. Previously, only the presence of aneuploid could be confirmed by conventional karyotyping of fetuses with thick nuchal... -
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- Prenatally Diagnosed and Surviving Patient with Jarcho-Levin Syndrome: Case Report with Literature Review
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Lee CY, Lee NM, Yi DY, Yun SW, Chae SA, Lim IS, Kim GJ
- KMID: 2430223
- Perinatology.
- 2018 Dec;29(4):185-188.
- doi: 10.14734/PN.2018.29.4.185
Jarcho-Levin syndrome is a congenital disorder characterized by several vertebral and costal anomalies. Other abnormalities have also been described, including neural tube defects, Arnold-Chiari malformation, renal/urinary tract abnormalities, hydrocephalus, hydroureteronephrosis,... -
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- Change in rates of prenatal tests for chromosomal abnormality over a 12-year period in women of advanced maternal age
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Kim SM, Kim HH, Han YJ, Choi JS, Ryu HM, Yang S, Kim MH
- KMID: 2439718
- Obstet Gynecol Sci.
- 2018 Jul;61(4):453-460.
- doi: 10.5468/ogs.2018.61.4.453
OBJECTIVE: In 2007, the American College of Obstetricians and Gynecologists (ACOG) recommended that all pregnant women be offered screening or diagnostic tests for chromosomal abnormalities regardless of their age. Noninvasive... -
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