1.Congenital Chloride Diarrhea in 5 Korean Infants.
Dong Hun RHIE ; Sun Hwan BAE ; Ji Eun CHOI ; Bo Young YUN ; Dong Woo SON ; Choong Ho SHIN ; Kyung Hee PARK ; Jae Sung KO ; Jeong Kee SEO
Journal of the Korean Pediatric Society 2000;43(11):1465-1472
PURPOSE: Congenital chloride diarrhea(CLD) is an autosomal recessive disease characterized by life-long watery diarrhea of prenatal onset with high fecal Cl concentration. Recent studies have revealed that the protein product of the down-regulated in adenoma(DRA) gene is an intestinal anion transporter molecule and causes CLD when mutatec4: We investigated the clinical characteristics of CLD in Korean infants in order to increase awareness of this disease, which might be simply overlooked as chronic diarrhea. METHODS: Medical records of 5 infants admitted to the pediatric departments of Eulji Medical Center and Seoul National 1Jniversity Children's Hospital from April 1988 to January 1998 with the diagnosis of CLD were retrospectively reviewed. The criteria for inclusion in the study were based on a typical clinical picture and high fecal Cl RESULTS: There were 4 boys and 1 girl, 2 of them were siblings with no consanguinity in their parents. Their ages ranged from birth to l4 months. The mean gestational age was 36 weeks and the mean birth weight was 2.99kg. In all patients abdominal distension, jaundice and watery diarrhea with a history of maternal polyhydramnios were found, lack of meconium passage was also documented and fecal Cl levels were greater than 90mmol/L. Three patients who were diagnosed beyond neonatal period had retarded growth and delayed development and presented hypochloremic hypokalernic dehydration. Two of thern were in a state of metabolic alkalosis. CONCLUSION: CLD should be considered in infants presenting with intractable watery diarrhea, abdominal distension, prematurity and history of polyhydramnios. Full replacement of the fecal losses of electrolytes ancl water can correct hypoelectrolyternic dehydration and will abolish[all the secondary] disorders. In this study we can be aware that with early detection and appropriate therapy infants with CLI) will achieve adequate growth and development.
Alkalosis
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Birth Weight
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Consanguinity
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Dehydration
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Diagnosis
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Diarrhea*
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Electrolytes
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Failure to Thrive
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Female
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Gestational Age
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Growth and Development
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Humans
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Infant*
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Jaundice
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Meconium
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Medical Records
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Parents
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Parturition
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Polyhydramnios
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Retrospective Studies
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Seoul
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Siblings
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Water
2.Regulation of osteogenic differentiation of human adipose-derived stem cells by controlling electromagnetic field conditions.
Kyung Shin KANG ; Jung Min HONG ; Jo A KANG ; Jong Won RHIE ; Young Hun JEONG ; Dong Woo CHO
Experimental & Molecular Medicine 2013;45(1):e6-
Many studies have reported that an electromagnetic field can promote osteogenic differentiation of mesenchymal stem cells. However, experimental results have differed depending on the experimental and environmental conditions. Optimization of electromagnetic field conditions in a single, identified system can compensate for these differences. Here we demonstrated that specific electromagnetic field conditions (that is, frequency and magnetic flux density) significantly regulate osteogenic differentiation of adipose-derived stem cells (ASCs) in vitro. Before inducing osteogenic differentiation, we determined ASC stemness and confirmed that the electromagnetic field was uniform at the solenoid coil center. Then, we selected positive (30/45 Hz, 1 mT) and negative (7.5 Hz, 1 mT) osteogenic differentiation conditions by quantifying alkaline phosphate (ALP) mRNA expression. Osteogenic marker (for example, runt-related transcription factor 2) expression was higher in the 30/45 Hz condition and lower in the 7.5 Hz condition as compared with the nonstimulated group. Both positive and negative regulation of ALP activity and mineralized nodule formation supported these responses. Our data indicate that the effects of the electromagnetic fields on osteogenic differentiation differ depending on the electromagnetic field conditions. This study provides a framework for future work on controlling stem cell differentiation.
Adipose Tissue/*cytology
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Alkaline Phosphatase/metabolism
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Biological Markers/metabolism
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Bone Matrix/metabolism
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Calcification, Physiologic/genetics
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*Cell Differentiation/genetics
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Core Binding Factor Alpha 1 Subunit/metabolism
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*Electromagnetic Fields
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Humans
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*Osteogenesis/genetics
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Reproducibility of Results
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Stem Cells/*cytology/enzymology/metabolism