1.An unusual combination of trisomy 21 and partial trisomy 5q.
Chong Jai KIM ; Je Geun CHI ; Kyu Hyung LEE ; Chun Kun LEE ; Myung Su YOO ; Yong Kyun PAIK
Journal of Korean Medical Science 1992;7(4):373-376
The authors describe a male newborn with multiple congenital anomalies; craniofacial dysmorphism, bilateral cleft palate and lip, ambiguous external genitalia with absence of phallus, ventricular septal defect, agenesis of olfactory bulbs, and presence of small round cells simulating migration defect in the cerebellar white matter. Cytogenetic study demonstrated a chromosomal constitution of 47,XY, +21, +5q. Its pathological significance compared with Down's syndrome and hitherto reported partial trisomy 5q is discussed.
Abnormalities, Multiple/*genetics/pathology
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*Chromosomes, Human, Pair 5
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Down Syndrome/*genetics/pathology
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Humans
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Infant, Newborn
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Male
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Phenotype
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*Trisomy
2.Isolated Non-chylous Pleural Effusion in Two Neonates.
Ji Young HWANG ; Jeong Hyun YOO ; Jeong Soo SUH ; Chung Sik RHEE
Journal of Korean Medical Science 2003;18(4):603-605
Isolated pleural effusion, so called primary pleural effusion denotes a pleural effusion without documented etiology such as a cardiac, inflammatory, iatrogenic problem or fetal hydrops. Chromosomal anomaly such as Down syndrome may be associated with isolated pleural effusion. The content of the isolated pleural effusion is mostly chylous, and isolated non-chylous pleural effusion in neonate is rare. We experienced 2 cases of isolated non-chylous pleural effusion. They had neither cardiac problem nor other sign of hydrops fetalis. Imaging diagnosis was done by plain chest radiography and subsequent ultrasonogram. One of them was diagnosed to Down syndrome by karyotyping. They were fared well after diagnostic and therapeutic thoracentesis. We describe 2 cases of non-chylous pleural effusion and review a few English-language case reports of this entity.
Chyloperitoneum/pathology
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Chylothorax/pathology
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Down Syndrome/diagnosis/genetics
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Female
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Fetal Diseases/diagnosis/therapy
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Gestational Age
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Human
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Hydrothorax
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Infant, Newborn
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Karyotyping
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Male
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*Pleural Effusion
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Pregnancy
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Ultrasonography
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Ultrasonography, Prenatal
3.Clinical and cytogenetic features of hematologic malignancies associated with acquired trisomy 21.
Huanping WANG ; Wanmao NI ; Zhimei CHEN ; Jiyu LOU ; Huan XU ; Yunbiao YU ; Wenbin QIAN ; Jie JIN
Chinese Journal of Medical Genetics 2008;25(5):576-578
OBJECTIVETo investigate the association between trisomy 21 abnormalities and the clinical and cytogenetic features of hematologic malignancies.
METHODSChromosome preparations were made on bone marrow cells by using direct method and/or unstimulated short-term cultures. Karyotypes were analyzed by R-banding.
RESULTSThirteen patients (1.5%) with acute myeloid leukemia (AML) including 6 cases of M5b, 8 (2.2%) with acute lymphoblastic leukemia (ALL) and 4 cases with other hematologic malignancies had acquired trisomy 21, and in 13 patients it occurred as the sole cytogenetic abnormality. The remaining had combination with other abnormalities. The median survival for the 19 patients with trisomy 21 was 9 months.
CONCLUSIONM5b was the major type in AML with sole acquired trisomy 21.Trisomy 21 as the sole abnormality appeared to have a poor prognosis.
Adolescent ; Adult ; Aged ; Down Syndrome ; complications ; Female ; Follow-Up Studies ; Hematologic Neoplasms ; complications ; genetics ; pathology ; Humans ; Karyotyping ; Leukemia, Myeloid, Acute ; complications ; genetics ; pathology ; Male ; Middle Aged ; Phenotype ; Precursor Cell Lymphoblastic Leukemia-Lymphoma ; complications ; genetics ; pathology ; Survival Rate
4.A Case of Pentasomy 21 With Two Isochromosome 21s in Acute Megakaryoblastic Leukemia Associated With Down Syndrome.
Yeongchun PARK ; Jinsook LIM ; Yong Hyun KO ; Jimyung KIM ; Gye Cheol KWON ; Sun Hoe KOO
Annals of Laboratory Medicine 2015;35(3):373-375
No abstract available.
*Aneuploidy
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Bone Marrow/pathology
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Chromosomes, Human, Pair 21
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Down Syndrome/*complications
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Female
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Humans
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Hyperplasia/pathology
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In Situ Hybridization, Fluorescence
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Infant
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Isochromosomes/*genetics
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Karyotype
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Leukemia, Megakaryoblastic, Acute/complications/*diagnosis
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Megakaryocytes/pathology
5.Haoqin Qingdan Decoction () and ribavirin therapy downregulate CD14 and toll-like receptor 4 in febrile disease with dampness-heat syndrome in a mouse model.
Huan-Huan LUO ; Feng-Xue ZHANG ; Wei WU ; Xin-Hua WANG
Chinese journal of integrative medicine 2016;22(10):768-773
OBJECTIVETo evaluate the effect of Chinese medicine Haoqin Qingdan Decoction (, HQD) for febrile disease dampness-heat syndrome (FDDHS).
METHODSForty mice were divided into four groups, including normal control, FDDHS (induced by Radix et Rhizoma Rhei recipe and influenza virus A1 FM1 model), HQD, and the ribavirin groups (10 in each). The normal control and FDDHS groups were administered normal saline. HQD and the ribavirin groups were administered HQD and ribavirin intragastrically once daily at a dose of 64 g/(kg d) and 0.07 g/(kg d), respectively for 7 days. Lethargy, rough hair, diarrhea, tongue color and sole color were evaluated for pathological changes in morphology. The tongue and lung tissues were collected for histology. The CD14 and toll-like receptor 4 (TLR4) expression levels were measured using real-time quantitative polymerase chain reaction.
RESULTSMore than 80% of the FDDHS mice showed hypokinesia and lethargy, and pathological changes associated with rough hair, diarrhea, tongue color and sole color. With advanced treatment for 7 days, the thick greasy tongue fur of the HQD and ribavirin groups were thinner than that of the FDDHS group (P<0.05), and it was the thinnest in the ribavirin group as compared with that in other groups (P<0.05). The CD14 and TLR4 expression levels in the lung tissues of HQD and ribavirin groups significantly delined compared with the model group (P<0.05 or P<0.01). CD14 was down-regulated more remarkably in the HQD group compared with the ribavirin group (P<0.05), whereas the converse was true with TLR4 (P<0.05).
CONCLUSIONSWe established a FDDHS mouse model showing systemic clinical symptoms. Both HQD and ribavirin can inhibit the expression of CD14 and TLR4 in FDDHS mice, while the effect of ribavirin might be much more violent. The expression changes of CD14 and TLR4 consistently refers to lipopolysaccharide, the commonly and hotly inducing factor in FDDHS.
Animals ; Behavior, Animal ; Disease Models, Animal ; Down-Regulation ; drug effects ; Drugs, Chinese Herbal ; pharmacology ; therapeutic use ; Fever ; drug therapy ; pathology ; Gene Expression Profiling ; Lipopolysaccharide Receptors ; genetics ; metabolism ; Lung ; drug effects ; pathology ; Mice, Inbred BALB C ; Ribavirin ; pharmacology ; therapeutic use ; Syndrome ; Toll-Like Receptor 4 ; genetics ; metabolism
6.Down syndrome critical region 1 enhances the proteolytic cleavage of calcineurin.
Ji Eun LEE ; Hyonchol JANG ; Eun Jung CHO ; Hong Duk YOUN
Experimental & Molecular Medicine 2009;41(7):471-477
Down syndrome critical region 1 (DSCR1), an oxidative stress-response gene, interacts with calcineurin and represses its phosphatase activity. Recently it was shown that hydrogen peroxide inactivates calcineurin by proteolytic cleavage. Based on these facts, we investigated whether oxidative stress affects DSCR1-mediated inactivation of calcineurin. We determined that overexpression of DSCR1 leads to increased proteolytic cleavage of calcineurin. Convertsely, knockdown of DSCR1 abolished calcineurin cleavage upon treatment with hydrogen peroxide. The PXIIXT motif in the COOH-terminus of DSCR1 is responsible for both binding and cleavage of calcineurin. The knockdown of overexpressed DSCR1 in DS fibroblast cells also abrogated calcineurin proteolysis by hydrogen peroxide. These results suggest that DSCR1 has the ability to inactivate calcineurin by inducing proteolytic cleavage of calcineurin upon oxidative stress.
Adenoviridae/genetics
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Adult
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Animals
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Calcineurin/antagonists & inhibitors/*metabolism
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Cells, Cultured
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Chromatin Immunoprecipitation
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Down Syndrome/*metabolism/pathology
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Fibroblasts/metabolism/pathology
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Humans
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Hydrogen Peroxide/pharmacology
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Immunoglobulin G/immunology
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Intracellular Signaling Peptides and Proteins/*physiology
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Male
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Mice
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Mice, Inbred ICR
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Muscle Proteins/*physiology
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Neuroblastoma/genetics/metabolism/pathology
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Neurons/cytology/metabolism
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Oxidants/pharmacology
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Oxidative Stress
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Peptide Fragments/immunology
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RNA, Messenger/genetics/metabolism
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RNA, Small Interfering/pharmacology
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Rabbits
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Reverse Transcriptase Polymerase Chain Reaction
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Skin/pathology
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Young Adult