- Causes and Clinical Features of Transient Hypocalcemia in Newborn: A Single Center Study
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Song BJ, Kim HS, Kim WD
- KMID: 2350282
- Neonatal Med.
- 2016 Aug;23(3):137-142.
- doi: 10.5385/nm.2016.23.3.137
PURPOSE: To review clinical symptoms, laboratory findings, and treatment of transient neonatal hypocalcemia. METHODS: Medical records of full-term (gestational age ≥37 weeks) neonates diagnosed with hypocalcemia, aged -
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- A Rare Case of Cerebral Sinovenous Thrombosis Associated with MTHFR A1298C and C677T Mutations
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Kim SH, Lee NM, Chae SA
- KMID: 2350287
- Neonatal Med.
- 2016 Aug;23(3):168-172.
- doi: 10.5385/nm.2016.23.3.168
Neonatal cerebral sinovenous thrombosis (CSVT) is a rare disease with severe neurological sequelae. Methylenetetrahydrofolate reductase (MTHFR) is a key enzyme in the folate cycle, and mutations in MTHFR are associated... -
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- Identification of a Novel Nonsense Mutation in the ARSE Gene of a Patient with X-Linked Recessive Chondrodysplasia Punctata
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Doo JW, Jang JH, Cho EH, Kim JK, Cho SC
- KMID: 2350289
- Neonatal Med.
- 2016 Aug;23(3):178-182.
- doi: 10.5385/nm.2016.23.3.178
X-linked recessive chondrodysplasia punctata (CDPX1) is caused by a hemizygous mutation in the arylsulfatase E (ARSE) gene located on chromosome Xp22.3. It is a rare congenital disorder of punctate calcifications... -
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- Clinical Characteristics of Patients with Bronchopulmonary Dysplasia Admitted to Pediatric Intensive Care Unit
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Choi YC, Jhang WK, Park SJ
- KMID: 2350284
- Neonatal Med.
- 2016 Aug;23(3):151-157.
- doi: 10.5385/nm.2016.23.3.151
PURPOSE: As the incidence of bronchopulmonary dysplasia (BPD) has increased, it is important to understand the clinical outcomes of BPD patients discharged from neonatal intensive care units (NICU). The purpose... -
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- A Case of Spontaneous Twin Anemia-Polycythemia Sequence
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Myung KD, Lee YK, Ko SY, Shin SM, Chung JH, Hong SR
- KMID: 2350286
- Neonatal Med.
- 2016 Aug;23(3):163-167.
- doi: 10.5385/nm.2016.23.3.163
Twin anemia-polycythemia sequence (TAPS) is characterized by the transfer of blood via intertwin vascular anastomoses in a single placenta. It differs from twin-twin transfusion syndrome (TTTS) in that amniotic fluid... -
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- Successful Peritoneal Dialysis in an Extremely Preterm Infant
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Huh J, Hwang J, Lee EH, Boo YJ, Choi BM, Hong YS
- KMID: 2350285
- Neonatal Med.
- 2016 Aug;23(3):158-162.
- doi: 10.5385/nm.2016.23.3.158
Peritoneal dialysis can be considered renal supportive therapy, even in an extremely low birth weight infant with acute kidney injury not responding to general supportive measures. Although there have been... -
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- The Clinical Features and Prognosis of Nephrocalcinosis in Preterm Neonates: A Single Center Study in Korea
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Lee H, Shim SY, Park EA, Cho SJ
- KMID: 2350281
- Neonatal Med.
- 2016 Aug;23(3):131-136.
- doi: 10.5385/nm.2016.23.3.131
PURPOSE: Nephrocalcinosis (NC) is frequently observed in premature infants. Small-scale studies have suggested that NC adversely affects renal function; however, the etiologic factors are still unclear. This prospective observational study... -
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- Vitamin D Status in Early Preterm Infants
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Lee JE, Lee WK, Jeon GW, Sin JB
- KMID: 2350283
- Neonatal Med.
- 2016 Aug;23(3):143-150.
- doi: 10.5385/nm.2016.23.3.143
PURPOSE: Vitamin D deficiency is still common in pregnant women and infants, especially preterm infants. This study evaluated the prevalence, characteristics, and prenatal and postnatal complications associated with vitamin D... -
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- Merosin-Deficient Congenital Muscular Dystrophy with Polymicrogyria and Subcortical Heterotopia: A Case Report
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Han YM, Lee NR, Bae MH, Park KH, Shin JH, Kim DS, Byun SY
- KMID: 2350288
- Neonatal Med.
- 2016 Aug;23(3):173-177.
- doi: 10.5385/nm.2016.23.3.173
This paper reports the brain magnetic resonance imaging (MRI) findings of a case of merosin-deficient congenital muscular dystrophy (MDCMD) in a neonate and discusses the spectrum of brain involvement in... -
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