- Proximal 16p11.2 Deletion in a Term Infant with Unilateral Microtia and Aural Atresia: A Case Report
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Kim J, Kim WD
- KMID: 2533893
- Perinatology.
- 2022 Sep;33(3):166-169.
- doi: 10.14734/PN.2022.33.3.166
The 16p11.2 deletion phenotype is characterized by developmental delays, intellectual disability and autistic features. In addition, the deletion of 16p11.2 is associated with epilepsy and obesity in childhood. We have... -
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- Fetus Prenatally Diagnosed with Lobar Holoprosencephaly Postnatally Diagnosed with Simple Hydrocephalus with Good Prognosis: A Case Report
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Moon H, Kim EH
- KMID: 2533894
- Perinatology.
- 2022 Sep;33(3):170-173.
- doi: 10.14734/PN.2022.33.3.170
Hydrocephalus is ventriculomegaly caused by an increased pressure of the cerebrospinal fluid within the ventricles of the brain. As uncomplicated hydrocephalus rarely has fatal outcomes, it stands in contrast to... -
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- Management and 2 Years Follow-Up of Newborns in the Neonatal Intensive Care Unit Exposed to Congenital Tuberculosis
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Yang JH, Lee JS, Song ES
- KMID: 2533891
- Perinatology.
- 2022 Sep;33(3):152-157.
- doi: 10.14734/PN.2022.33.3.152
Objective: We report the management and 2 years follow-up of newborns in the neonatal intensive care unit (NICU) exposed to congenital tuberculosis (Tb). Methods: Preterm twins born to a mother diagnosed... -
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- Unexplained Marked Elevation of Serum Transaminase Levels in the Third Trime ster of Pregnancy, with Half of the Cases Suspicious of Intrahepatic Cholestasis of Pregnancy
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Lim SH, Kim R, Kang HS, Shim SS
- KMID: 2533892
- Perinatology.
- 2022 Sep;33(3):158-165.
- doi: 10.14734/PN.2022.33.3.158
Objective: Major causes of markedly elevated serum transaminase levels in the third trimester of pregnancy are severe preeclampsia, HELLP (hemolysis, elevated liver enzymes, and low platelet counts) syndrome, viral hepatitis,... -
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- Chromosomal Microarray Analysis and Pre natal Diagnosis: What Obstetricians Should Know
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Son H, Choi ES, Ju Y, Park JS, Lee SM
- KMID: 2533887
- Perinatology.
- 2022 Sep;33(3):121-126.
- doi: 10.14734/PN.2022.33.3.121
Chromosomal microarray (CMA) is a high-resolution technique that can analyze the entire genome and can detect submicroscopic aberration. CMA can be performed in prenatal settings by using fetal DNA. Compared... -
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- Clinical Characteristics of Symptomatic Rotavirus Infection in Newborn Infants and Genotype Analysis
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Kim DS, Byun JC, Ryoo NH, Kim CS
- KMID: 2533890
- Perinatology.
- 2022 Sep;33(3):143-151.
- doi: 10.14734/PN.2022.33.3.143
Objective: Clinical data on rotavirus infection in the neonatal period are still limited. In this study, we investigated the incidence and monthly distribution, clinical features, and genotypes of symptomatic rotavirus... -
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- Unsupervised Clustering of Late Preterm Infants in Terms of Developmental Outcome
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Kim H, Song JH, Kim SS
- KMID: 2533888
- Perinatology.
- 2022 Sep;33(3):127-135.
- doi: 10.14734/PN.2022.33.3.127
Objective: This study aimed to derive the subtype of late preterm infants (gestational age, 34 to 36 weeks) according to their developmental outcomes. Methods: We retrospectively investigated the medical records of... -
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- The Success of Brain Magnetic Resonance Imaging in Non-Sedated Infants
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Yu NL, Lee HM, Kim HG, Kim SY
- KMID: 2533889
- Perinatology.
- 2022 Sep;33(3):136-142.
- doi: 10.14734/PN.2022.33.3.136
Objective: This study aimed to evaluate the success rate of brain magnetic resonance imaging (MRI) in non-sedated at a single neonatal intensive care unit (NICU). Methods: Infants underwent brain MRI following... -
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