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Journal articles on the topic 'Down syndrome'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Duchoslavová, Lenka. "Down syndrome." Kontakt 9, no. 2 (2007): 416–21. http://dx.doi.org/10.32725/kont.2007.063.

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2

Hobson-Rohrer, W. L., and L. Samson-Fang. "Down Syndrome." Pediatrics in Review 34, no. 12 (2013): 573–74. http://dx.doi.org/10.1542/pir.34-12-573.

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3

Hobson-Rohrer, Wendy L., and Lisa Samson-Fang. "Down Syndrome." Pediatrics In Review 34, no. 12 (2013): 573–74. http://dx.doi.org/10.1542/pir.34.12.573.

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4

DAVIES, M. K., and A. HOLLMAN. "Down syndrome." Heart 86, no. 2 (2001): 130. http://dx.doi.org/10.1136/hrt.86.2.130.

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5

Bull, Marilyn J. "Down Syndrome." New England Journal of Medicine 382, no. 24 (2020): 2344–52. http://dx.doi.org/10.1056/nejmra1706537.

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6

&NA;. "DOWN SYNDROME." Advances in Neonatal Care 9, no. 1 (2009): 31–33. http://dx.doi.org/10.1097/01.anc.0000346093.50981.89.

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7

Prasher, Vee, and Cliff Cunningham. "Down syndrome." Current Opinion in Psychiatry 14, no. 5 (2001): 431–36. http://dx.doi.org/10.1097/00001504-200109000-00002.

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8

SMITH, JEAN C., WILLIAM L. COLEMAN, ADRIAN D. SANDLER, and CATHERINE L. GRUS. "DOWN SYNDROME." Journal of Developmental & Behavioral Pediatrics 18, no. 2 (1997): 134. http://dx.doi.org/10.1097/00004703-199704000-00021.

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9

Crain, Lucy S. "Down Syndrome." Journal of Developmental & Behavioral Pediatrics 20, no. 4 (1999): 297. http://dx.doi.org/10.1097/00004703-199908000-00016.

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10

Van Dyke, Don C., and Cheryl A. Gahagan. "Down Syndrome." Clinical Pediatrics 27, no. 9 (1988): 415–18. http://dx.doi.org/10.1177/000992288802700901.

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11

Caputo, Anthony R., Rudolph S. Wagner, David R. Reynolds, Suqin Guo, and Ameet K. Goel. "Down Syndrome." Clinical Pediatrics 28, no. 8 (1989): 355–58. http://dx.doi.org/10.1177/000992288902800804.

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12

RIMMERMAN, ARIE. "Down Syndrome." International Journal of Rehabilitation Research 17, no. 3 (1994): 278. http://dx.doi.org/10.1097/00004356-199409000-00010.

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13

DAVIES, M. K. "Down syndrome." Heart 86, no. 2 (2001): 130. http://dx.doi.org/10.1136/heart.86.2.130.

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14

Hayes, Adadot, and Mark L. Batshaw. "Down Syndrome." Pediatric Clinics of North America 40, no. 3 (1993): 523–35. http://dx.doi.org/10.1016/s0031-3955(16)38548-0.

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15

Desai, Sindoor S. "Down syndrome." Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology 84, no. 3 (1997): 279–85. http://dx.doi.org/10.1016/s1079-2104(97)90343-7.

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16

Baird, PA. "Down syndrome." Biomedicine & Pharmacotherapy 44, no. 1 (1990): 62. http://dx.doi.org/10.1016/0753-3322(90)90076-l.

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17

&NA;. "DOWN SYNDROME." Plastic and Reconstructive Surgery 82, no. 1 (1988): 200. http://dx.doi.org/10.1097/00006534-198807000-00057.

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18

&NA;. "DOWN SYNDROME." Plastic and Reconstructive Surgery 82, no. 1 (1988): 200. http://dx.doi.org/10.1097/00006534-198882010-00057.

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19

Capone, George T. "Down Syndrome." Infants & Young Children 17, no. 1 (2004): 45–58. http://dx.doi.org/10.1097/00001163-200401000-00007.

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20

Takashima, Sachio. "Down syndrome." Current Opinion in Neurology 10, no. 2 (1997): 148–52. http://dx.doi.org/10.1097/00019052-199704000-00013.

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21

Amirfeyz, Rouin, Demetris Aspros, and Martin Gargan. "Down syndrome." Current Orthopaedics 20, no. 3 (2006): 212–15. http://dx.doi.org/10.1016/j.cuor.2006.01.003.

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22

Kava, Maina P., Milind S. Tullu, Mamta N. Muranjan, and K. M. Girisha. "Down syndrome:." Archives of Medical Research 35, no. 1 (2004): 31–35. http://dx.doi.org/10.1016/j.arcmed.2003.06.005.

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23

Bianca, Sebastiano, and M. Bianca. "Down Syndrome." Archives of Medical Research 36, no. 2 (2005): 183. http://dx.doi.org/10.1016/j.arcmed.2004.12.017.

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24

Catalano, Robert A. "Down syndrome." Survey of Ophthalmology 34, no. 5 (1990): 385–98. http://dx.doi.org/10.1016/0039-6257(90)90116-d.

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25

Dr. Apte M. V, Dr Apte M. V., and Dr Suresh D. Gangane. "Clinical Profile of Down Syndrome Cases." International Journal of Scientific Research 2, no. 2 (2012): 273–74. http://dx.doi.org/10.15373/22778179/feb2013/91.

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26

Marques Silva, Lilian, Maria Lucia Pereira da, Eik Tenorio, and Volney Mattos de Oliveira. "Living and Learning with Down Syndrome." International Journal of Science and Research (IJSR) 10, no. 7 (2021): 1117–24. https://doi.org/10.21275/sr21427004518.

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27

Wei, Miao, Natasha Lepore, Kelli Paulsen, and Jonathan D. Santoro. "Down syndrome with co-occurring Marfan syndrome." BMJ Case Reports 13, no. 9 (2020): e235988. http://dx.doi.org/10.1136/bcr-2020-235988.

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Down syndrome (DS) and Marfan syndrome (MFS) are two unique genetic disorders that share limited phenotypic overlap. There are very few reported cases in the existing literature on overlapping DS and MFS. Although these two disorders are phenotypically unique, features present in these cases are variable, resulting in mixed and dominant expressions of particular features. We present the first adolescent case of trisomy 21 associated DS and fibrillin-1 gene associated MFS in the literature who had a height at 90th percentile for an 11-year old boy and discuss the implications of this case in te

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28

Sun, Deborah H., and Julius Kerkay. "Correlation of the Down Syndrome Protein with Down Syndrome." Analytical Letters 23, no. 5 (1990): 819–31. http://dx.doi.org/10.1080/00032719008052484.

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29

Merve, Çaylı*, Kutlu Yakup, and Yeroğlu Celaleddin. "Identification of Individuals With Down Syndrome Using Pre-Trained Models." Journal of Intelligent Systems with Applications 7, no. 2 (2024): 19–23. https://doi.org/10.5281/zenodo.14585490.

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Down syndrome is a genetic disorder and is caused by an extra copy of the 21st chromosome. This extra genetic material causes the physical and developmental characteristics associated with Down syndrome. It is known that the quality of life of individuals can be increased with developing robotic technology. This situation can be used to customize for individuals with Down syndrome, to enable them to adapt to social life more easily and to reveal their potential. The aim of the paper is to detect individuals with Down syndrome and to enable approaching these individuals differently. The outputs

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30

Ulfah, Siti Fitria. "SOCIAL SUPPORT ORANG TUA DOWN SYNDROME BERDASARKAN KARAKTERISTIK TINGKAT PENDIDIKAN DAN PEKERJAAN." Jurnal Kesehatan Gigi dan Mulut (JKGM) 6, no. 2 (2024): 206–12. https://doi.org/10.36086/jkgm.v6i2.2430.

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Latar belakang: Down Syndrom merupakan kondisi genetik yang menyebabkan berbagai tantangan dalam perkembangan fisik dan intelektual. Down syndrom seringkali tidak dapat menjaga kebersihan mulut mereka sendiri, yang dapat menyebabkan masalah kesehatan gigi seperti penyakit periodontal. Oleh karena itu social support dari orangtua sangat dibutuhkan untuk mengatasi kesulitan dalam pemeliharaan kesehatan gigi mereka. Tujuan dari penelitian ini adalah menganalisis social support yang diterima oleh orang tua yang memiliki anak Down Syndrome berdasarkan karakteristik level pendidikan dan pekerjaan. M

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31

Szatkowska, Marta, Dominika Zimny, and Ewa Barg. "Down syndrome and hyperthyroidism – two case reports." Pediatric Endocrinology Diabetes and Metabolism 21, no. 2 (2015): 93–96. http://dx.doi.org/10.18544/pedm-21.02.0030.

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32

Makwana, Mohan, Vishnoi R.K, Jai Prakash Soni, et al. "DOWN SYNDROME WITH MOYAMOYA SYNDROME." Journal of Evidence Based Medicine and Healthcare 4, no. 29 (2017): 1735–37. http://dx.doi.org/10.18410/jebmh/2017/338.

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33

Berg, Joseph M., and Marika Korossy. "Down syndrome before down: A retrospect." American Journal of Medical Genetics 102, no. 2 (2001): 205–11. http://dx.doi.org/10.1002/1096-8628(20010801)102:2<205::aid-ajmg1454>3.0.co;2-c.

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34

Berg, Joseph M. "Down syndrome before down: A postscript." American Journal of Medical Genetics 116A, no. 1 (2002): 97–98. http://dx.doi.org/10.1002/ajmg.a.10840.

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35

Buckley, Frank. "Modelling Down syndrome." Down Syndrome Research and Practice 12, no. 2 (2008): 98–102. http://dx.doi.org/10.3104/updates.2054.

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36

Kumar Agrawal, Adesh. "Scroll Down Syndrome." Journal of Anxiety & Depression 5, no. 1 (2022): 144. http://dx.doi.org/10.46527/2582-3264.144.

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37

Cooper, Lucienne, and Nicola Enoch. "Down syndrome training." British Journal of Midwifery 30, no. 8 (2022): 428–29. http://dx.doi.org/10.12968/bjom.2022.30.8.428.

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38

Maurice Delabar, Jean. "Syndrome de Down." médecine/sciences 26, no. 4 (2010): 371–76. http://dx.doi.org/10.1051/medsci/2010264371.

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39

Riou, Morgan. "Down syndrome screening." Vocation Sage-femme 18, no. 139 (2019): 45–47. http://dx.doi.org/10.1016/j.vsf.2019.05.010.

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40

Palumbo, Michelle. "54.4 DOWN SYNDROME." Journal of the American Academy of Child & Adolescent Psychiatry 59, no. 10 (2020): S83. http://dx.doi.org/10.1016/j.jaac.2020.07.345.

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41

Feingold, Murray. "Down syndrome adults." American Journal of Medical Genetics 124A, no. 4 (2004): 416. http://dx.doi.org/10.1002/ajmg.a.20389.

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42

Roizen, Nancy J. "Overview: Down syndrome." Mental Retardation and Developmental Disabilities Research Reviews 2, no. 2 (1996): 65. http://dx.doi.org/10.1002/(sici)1098-2779(1996)2:2<65::aid-mrdd1>3.0.co;2-w.

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43

Stephenson, J. "Diagnosing Down Syndrome." JAMA: The Journal of the American Medical Association 286, no. 22 (2001): 2801—a—2801. http://dx.doi.org/10.1001/jama.286.22.2801-a.

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44

Stephenson, Joan. "Diagnosing Down Syndrome." JAMA 286, no. 22 (2001): 2801. http://dx.doi.org/10.1001/jama.286.22.2801-jwm10013-2-1.

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45

Hook, Ernest B., John M. Opitz, and James F. Reynolds. "Risk of down syndrome among relatives of down syndrome individuals." American Journal of Medical Genetics 22, no. 1 (1985): 213–14. http://dx.doi.org/10.1002/ajmg.1320220120.

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46

Kratz, Christian P., and Shai Izraeli. "Down syndrome, RASopathies, and other rare syndromes." Seminars in Hematology 54, no. 2 (2017): 123–28. http://dx.doi.org/10.1053/j.seminhematol.2017.04.008.

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47

Bihunyak, T. V., Yu I. Bondarenko, O. O. Кulyanda, S. M. Charnosh, A. S. Sverstiuk, and K. O. Bihuniak. "CHROMOSOMAL DISEASES IN THE HUMAN PATHOLOGY." International Journal of Medicine and Medical Research 6, no. 1 (2020): 50–60. http://dx.doi.org/10.11603/ijmmr.2413-6077.2020.1.11501.

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Background. Chromosomal diseases are the cause of 45-50 % of multiple birth defects. Basic research on mutations is performed using genomic technologies to identify a correlation between genotype and phenotype in aneuploidies and to understand its pathogenesis. Objective. The aim of the research is to study the etiology, pathogenesis of symptoms and diagnostics for patients with Down, Klinefelter, Turner syndromes and double aneuploidies by 21 and sex chromosomes. Methods. A literature review by the keywords “Down syndrome”, “Klinefelter syndrome”, “Turner syndrome”, “double aneupl

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48

Isnawijayani, Isnawijayani. "KOMUNIKASI ORANGTUA UNTUK ANAK PENDERITA DOWN SYNDROME." Jurnal Inovasi 13, no. 1 (2019): 20–33. http://dx.doi.org/10.33557/jurnalinovasi.v13i1.608.

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The purpose of this study illustrate the Children who are born with disabilities or mental retardation. Has characteristics that are easily recognizable as mental retardation (mental obstacles), visual impairment (visual barriers), hearing impairment (hearing barriers), physical impairment (disability). Seen as a useless person. Not many people know that they can also be self-sufficient and achievement. Communication with parents to see children with Down Syndrome. With descriptive qualitative methods, this study using the Theory of Applied Behaviour Analysis (ABA) on Ivar O.Lavass to change d

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49

Fajar, Ibtesam-E., Taimur Khalil Sheikh, Huma Bashir Janjua, et al. "Conservative Management Techniques for Ideal Grooming and Upbringing of Downs Syndrome Children." Pakistan Journal of Medical and Health Sciences 16, no. 3 (2022): 1096–99. http://dx.doi.org/10.53350/pjmhs221631096.

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Introduction: Down syndrome are slow learners having mild to moderate intellectual disability with co-morbidities, we need to pay special attention on conservative management techniques like early intervention programs, speech therapies, physiotherapies, exercises, sports, schooling and education etc. to make these children intellectual, groomed and compatible for a normal life. Objective: To identify the conservative management techniques for improving the quality of life for down syndromes. Methodology: A descriptive cross-sectional survey (designed after literature search) was conducted fro

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50

Geta, Mitrea. "Preterm Low Birth Weight Down Syndrome and Mieloid Leukemia." J Biomed Res Environ Sci 3, no. 9 (2022): 1039–41. https://doi.org/10.37871/jbres1551.

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<strong>Introduction:</strong> Langdon Down syndrome (Trisomy 21) is the most common genetic syndrome compatible with survival. Down syndrome is a chromosomal condition characterized by the presence of an additional copy of the genetic material on chromosome 21, either in full (trisomy 21) or partially, due to a translocation. <strong>Objective: </strong>The importance of early detection of Down's Syndrome and highlighting the complications caused by this syndrome. Material and methods: In our study, we analyzed the case of a premature LBW (Low Birth Weight), SGA (small gestation

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