- Consideration of Sensory Aspect in Neonatal Care
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Sin JB
- KMID: 1876153
- Korean J Perinatol.
- 2006 Mar;17(1):1-11.
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- A Case of Beals-Hecht syndrome
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Bae WJ, Choi EK, Sin JB
- KMID: 2144545
- J Korean Soc Neonatol.
- 2005 Nov;12(2):222-226.
Beals-Hecht syndrome, also known as congenital contractural arachnodactyly, is a rare autosomal dominant, connective tissue disorder characterized by congenital joint contractures, arachnodactyly, dolichostenomelia, crumpled ear, and kyphoscoliosis. We report a... -
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- A case of hemimegalencephaly with congenital foot deformity
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Cheong YH, Park EA, Park KK, Jeon GW, Sin JB
- KMID: 2280783
- Korean J Perinatol.
- 2008 Sep;19(3):308-311.
Hemimegalencephaly is a rare congenital malformation of the cortical development arising from abnormal proliferation of anomalous neuronal and glial cells. The characteristic clinical manifestations are macrocephaly, psycomotor retardation, intractable seizure... -
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- Identification of Somatic KRAS Mutation in a Korean Baby with Nevus Sebaceus Syndrome
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Kim SW, Song JS, Kang MS, Sin JB, Ki CS, Jeon GW
- KMID: 2363174
- Ann Lab Med.
- 2015 Jan;35(1):178-180.
- doi: 10.3343/alm.2015.35.1.178
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- A Case of Congenital Epulis Arising from the Mandibular Gingiva
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Kwak NH, Jung JM, Jeon GW, Sin JB
- KMID: 1980171
- Korean J Perinatol.
- 2009 Jun;20(2):153-157.
Congenital epulis is a rare benign tumor occurring on the anterior maxillary gingiva, also known as granular cell tumor of the newborn or Neumann's tumor, which is seen only in... -
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- A Case of Congenital Right Diaphragmatic Eventration
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Byun JM, Kim YN, Jeong DH, Lee KB, Sung MS, Kim KT, Jeon GW, Sin JB
- KMID: 1472011
- Korean J Perinatol.
- 2009 Sep;20(3):254-259.
Congenital diaphragmatic eventration is defined as an abnormal elevation of the diaphragm resulting from developmental abnormality of muscle fibers during gestation. Differentiation between congenital diaphragmatic hernia (CDH) and eventration is... -
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- Left-Sided Gastroschisis: A Rare Congenital Abdominal Wall Defect
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Shin JH, Jeon GW, Sin JB
- KMID: 2312980
- Neonatal Med.
- 2015 Aug;22(3):168-172.
- doi: 10.5385/nm.2015.22.3.168
Gastroschisis is a congenital abdominal wall defect that occurs at the immediate right of the umbilicus. Left-sided gastroschisis, which is located in the left periumbilical region, is extremely rare, as... -
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- A case of Pfeiffer syndrome with c833_834GC>TG (Cys278Leu) mutation in the FGFR2 gene
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Lee MY, Jeon GW, Jung JM, Sin JB
- KMID: 2073610
- Korean J Pediatr.
- 2010 Jul;53(7):774-777.
- doi: 10.3345/kjp.2010.53.7.774
Pfeiffer syndrome is a rare autosomal dominant disorder characterized by coronal craniosynostosis, brachycephaly, mid-facial hypoplasia, and broad and deviated thumbs and great toes. Pfeiffer syndrome occurs in approximately 1:100,000 live... -
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- Kostmann's Disease: A Case Report
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Yoon CG, Jang JG, Sin JB, Lee SY
- KMID: 2072485
- Korean J Pediatr Hematol Oncol.
- 1999 Apr;6(1):136-140.
Kostmann's disease is a rare hematologic disease entity which is characterized by persistent neutropenia and recurrent bacterial infections since early in infancy. The authors experienced a 2-month-old female infant... -
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- A case of restrictive dermopathy
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Lee SI, Hong CH, Cheong YH, Kang MS, Sin JB
- KMID: 2279253
- Korean J Pediatr.
- 2007 Mar;50(3):306-310.
- doi: 10.3345/kjp.2007.50.3.306
Restrictive dermopathy is a rare autosomal recessive disorder in which rigidity or tautness of the skin from the second trimester causes a fetal akinesia deformation sequence (FADS) and early death.... -
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- The First Korean Case of Cutaneous Lung Tissue Heterotopia
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Jeon GW, Han SW, Jung JM, Kang MS, Sin JB
- KMID: 1785924
- J Korean Med Sci.
- 2010 Sep;25(9):1387-1389.
- doi: 10.3346/jkms.2010.25.9.1387
Cutaneous lung tissue heterotopia is a very rare disorder where mature lung tissues develop in the skin. This is only the second known report of cutaneous lung tissue heterotopia, with... -
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- Regionalization of neonatal care and neonatal transport system
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Sin JB
- KMID: 2278739
- Korean J Pediatr.
- 2007 Jan;50(1):1-6.
- doi: 10.3345/kjp.2007.50.1.1
In the United States, The concept of designation for hospital facilities that care for newborn infants according to the level of complexity of care provided was first proposed in 1976.... -
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- A case of SRY Negative 46, XX Male Syndrome with Deletion on Long Arm of X Chromosome
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Lee JW, Hong CH, Kim HR, Sin JB
- KMID: 2280592
- Korean J Perinatol.
- 2006 Sep;17(3):353-358.
46,XX male sex reversal syndrome is, also called the de la Chapelle syndrome, a rare cause of abnormal sex determination with an incidence of 1 in 20,000~25,000 male neonates. The... -
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- Enteral Feeding for Preterm Infants-Benefits and Risks
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Sin JB
- KMID: 2144484
- J Korean Soc Neonatol.
- 2009 Nov;16(2):121-130.
Over the past 20 years, neonatal mortality rates for preterm infants, particularly those born extremely preterm and with a very low birth weight, have decreased steadily. As more very immature... -
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- Associated Malformations and Chromosomal Defects in Antenatally Diagnosed Hydronephrosis
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Kwak NH, Han SW, Jung JM, Jeon GW, Sin JB
- KMID: 2072215
- Korean J Perinatol.
- 2009 Dec;20(4):354-360.
PURPOSE: With the increasing use of antenatal sonography, fetal hydronephrosis has been reported more frequently. But, despite extensive clinical and scientific research much controversy still exists about the assessment and... -
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- Pain reducing effect of vapocoolant spray during injection and heelstick procedure in neonates
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Choi EK, Jung JM, Sin JB
- KMID: 2280453
- Korean J Pediatr.
- 2008 May;51(5):481-486.
- doi: 10.3345/kjp.2008.51.5.481
Purpose: The aims of this study were to test the efficacy of vapocoolant spray to decrease the symptoms associated with pain in newborns undergoing heel stick and intramuscular injection and... -
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- Risk Factors of Failure of Ibuprofen Treatment in Preterm Infants with Hemodynamically Significant Patent Ductus Arteriosus
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Kwon NH, Lee JH, Jeon GW, Sin JB
- KMID: 2281143
- Korean J Perinatol.
- 2014 Dec;25(4):257-265.
- doi: 10.14734/kjp.2014.25.4.257
PURPOSE: In this study, the risk factors of failure of ibuprofen treatment in preterm infants with hemodynamically significant patent ductus arteriosus (hsPDA) were investigated. METHODS: Among 403 preterm infants ( -
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- VACTERL Association with Meningomyelocele Combined with Trisomy 18 Syndrome
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Kim YK, Lee JH, Jeon GW, Sin JB
- KMID: 2312962
- Neonatal Med.
- 2014 Feb;21(1):74-78.
Vertebral, anal, cardiac, tracheo-esophageal, renal, and limb(VACTERL) association is defined as the presence of at least three of the above-mentioned six manifestations. An estimated incidence of the VACTERL association is... -
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- A Case of Chromosome 1q44 Deletion with Microcephaly and Multiple Congenital Anomalies
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Lee JE, Jung JS, Jeon GW, Sin JB
- KMID: 2280960
- Korean J Perinatol.
- 2014 Jun;25(2):95-99.
- doi: 10.14734/kjp.2014.25.2.95
The 1q terminal deletion syndrome is a rare chromosomal disorder which was first reported by Mankinen et al. in 1976. This disorder has shown to have broad and diverse clinical... -
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- Risk Factors of Transfusion in Anemia of Very Low Birth Weight Infants
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Jeon GW, Sin JB
- KMID: 1503898
- Yonsei Med J.
- 2013 Mar;54(2):366-373.
- doi: 10.3349/ymj.2013.54.2.366
PURPOSE: Anemia of prematurity is frequent in preterm infants, for which red blood cell (RBC) transfusion remains the treatment of choice. In this study, we attempted to evaluate the characteristics... -
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