Trisomy 21 in visual art
In 1866, J. Langdon Down published a paper on "an ethnic classification of idiots" and noted their facial resemblance with individuals of the Mongolian people. In 1959, J. Lejeune, M. Gautier, and R. Turpin demonstrated that the children with Down syndrome had an extra copy of chromosome 2...
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Veröffentlicht in: | Archives de pédiatrie : organe officiel de la Société française de pédiatrie 2013-12, Vol.20 (12), p.1342-1351 |
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description | In 1866, J. Langdon Down published a paper on "an ethnic classification of idiots" and noted their facial resemblance with individuals of the Mongolian people. In 1959, J. Lejeune, M. Gautier, and R. Turpin demonstrated that the children with Down syndrome had an extra copy of chromosome 21. There is now a debate within the medical literature on the age of trisomy 21 as a disease affecting mankind. Since it was not described before 1866, some authors questioned whether this disease is an old or new condition in humans. Three methods of investigation are useful for demonstrating that trisomy 21 has been present in humans for a long time: the figuration of this condition in historical paintings, figurines, and pottery; its presence in old skeletal remains; and the origin of human chromosome 21 during primate phylogeny. Figurines strongly suggestive of trisomy 21 have been found in the Greco-Roman world, in many Central and South American pre-Columbian cultures, and in Khmer temples. In Europe, during the Renaissance, Italian and Flemish artists represented trisomy 21 in paintings of religious inspiration. Studies on the origin and pathology of chromosome 21 have shown that the ancestral human chromosome 21 arose 30-50 million years ago and that trisomy 21 has existed since time immemorial. |
doi_str_mv | 10.1016/j.arcped.2013.09.024 |
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Langdon Down published a paper on "an ethnic classification of idiots" and noted their facial resemblance with individuals of the Mongolian people. In 1959, J. Lejeune, M. Gautier, and R. Turpin demonstrated that the children with Down syndrome had an extra copy of chromosome 21. There is now a debate within the medical literature on the age of trisomy 21 as a disease affecting mankind. Since it was not described before 1866, some authors questioned whether this disease is an old or new condition in humans. Three methods of investigation are useful for demonstrating that trisomy 21 has been present in humans for a long time: the figuration of this condition in historical paintings, figurines, and pottery; its presence in old skeletal remains; and the origin of human chromosome 21 during primate phylogeny. Figurines strongly suggestive of trisomy 21 have been found in the Greco-Roman world, in many Central and South American pre-Columbian cultures, and in Khmer temples. In Europe, during the Renaissance, Italian and Flemish artists represented trisomy 21 in paintings of religious inspiration. Studies on the origin and pathology of chromosome 21 have shown that the ancestral human chromosome 21 arose 30-50 million years ago and that trisomy 21 has existed since time immemorial.</description><identifier>EISSN: 1769-664X</identifier><identifier>DOI: 10.1016/j.arcped.2013.09.024</identifier><identifier>PMID: 24210986</identifier><language>fre</language><publisher>France</publisher><subject>Archaeology - history ; Cambodia ; Central America ; Down Syndrome - history ; Europe ; History, 15th Century ; History, 16th Century ; History, 17th Century ; History, 18th Century ; History, 19th Century ; History, 20th Century ; History, 21st Century ; History, Ancient ; History, Medieval ; Humans ; Medicine in the Arts ; Paintings - history ; Roman World - history ; Sculpture - history ; South America</subject><ispartof>Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2013-12, Vol.20 (12), p.1342-1351</ispartof><rights>Copyright © 2013. 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Turpin demonstrated that the children with Down syndrome had an extra copy of chromosome 21. There is now a debate within the medical literature on the age of trisomy 21 as a disease affecting mankind. Since it was not described before 1866, some authors questioned whether this disease is an old or new condition in humans. Three methods of investigation are useful for demonstrating that trisomy 21 has been present in humans for a long time: the figuration of this condition in historical paintings, figurines, and pottery; its presence in old skeletal remains; and the origin of human chromosome 21 during primate phylogeny. Figurines strongly suggestive of trisomy 21 have been found in the Greco-Roman world, in many Central and South American pre-Columbian cultures, and in Khmer temples. In Europe, during the Renaissance, Italian and Flemish artists represented trisomy 21 in paintings of religious inspiration. Studies on the origin and pathology of chromosome 21 have shown that the ancestral human chromosome 21 arose 30-50 million years ago and that trisomy 21 has existed since time immemorial.</description><subject>Archaeology - history</subject><subject>Cambodia</subject><subject>Central America</subject><subject>Down Syndrome - history</subject><subject>Europe</subject><subject>History, 15th Century</subject><subject>History, 16th Century</subject><subject>History, 17th Century</subject><subject>History, 18th Century</subject><subject>History, 19th Century</subject><subject>History, 20th Century</subject><subject>History, 21st Century</subject><subject>History, Ancient</subject><subject>History, Medieval</subject><subject>Humans</subject><subject>Medicine in the Arts</subject><subject>Paintings - history</subject><subject>Roman World - history</subject><subject>Sculpture - history</subject><subject>South America</subject><issn>1769-664X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j8FLwzAYxYMgbk7vHkR69NLu-5L0S3KU4VQY7NKDt5ImGXS0a01WYf-9Eyfv8C6_34PH2CNCgYC03Bc2ujH4ggOKAkwBXF6xOSoyOZH8nLHblPYAoEGLGzbjkiMYTXP2UMU2Df0p45i1h-y7TZPtMhuPd-x6Z7sU7i-9YNX6tVq955vt28fqZZOPJVGOCjw6QzwoQV6Vylrk3kvdeCldIKcbpRtyXBmUhMHurDZaneNK0NKKBXv-mx3j8DWFdKz7NrnQdfYQhinVv5ZWyLk4o08XdGr64Osxtr2Np_r_jPgBM8ZIsA</recordid><startdate>201312</startdate><enddate>201312</enddate><creator>Stahl, A</creator><creator>Tourame, P</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201312</creationdate><title>Trisomy 21 in visual art</title><author>Stahl, A ; Tourame, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p566-170d1c962e736d757aa12dd48bd44ce6c8b78b6c2791461eafa8987878c5084a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>fre</language><creationdate>2013</creationdate><topic>Archaeology - history</topic><topic>Cambodia</topic><topic>Central America</topic><topic>Down Syndrome - history</topic><topic>Europe</topic><topic>History, 15th Century</topic><topic>History, 16th Century</topic><topic>History, 17th Century</topic><topic>History, 18th Century</topic><topic>History, 19th Century</topic><topic>History, 20th Century</topic><topic>History, 21st Century</topic><topic>History, Ancient</topic><topic>History, Medieval</topic><topic>Humans</topic><topic>Medicine in the Arts</topic><topic>Paintings - history</topic><topic>Roman World - history</topic><topic>Sculpture - history</topic><topic>South America</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stahl, A</creatorcontrib><creatorcontrib>Tourame, P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Archives de pédiatrie : organe officiel de la Société française de pédiatrie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stahl, A</au><au>Tourame, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trisomy 21 in visual art</atitle><jtitle>Archives de pédiatrie : organe officiel de la Société française de pédiatrie</jtitle><addtitle>Arch Pediatr</addtitle><date>2013-12</date><risdate>2013</risdate><volume>20</volume><issue>12</issue><spage>1342</spage><epage>1351</epage><pages>1342-1351</pages><eissn>1769-664X</eissn><abstract>In 1866, J. Langdon Down published a paper on "an ethnic classification of idiots" and noted their facial resemblance with individuals of the Mongolian people. In 1959, J. Lejeune, M. Gautier, and R. Turpin demonstrated that the children with Down syndrome had an extra copy of chromosome 21. There is now a debate within the medical literature on the age of trisomy 21 as a disease affecting mankind. Since it was not described before 1866, some authors questioned whether this disease is an old or new condition in humans. Three methods of investigation are useful for demonstrating that trisomy 21 has been present in humans for a long time: the figuration of this condition in historical paintings, figurines, and pottery; its presence in old skeletal remains; and the origin of human chromosome 21 during primate phylogeny. Figurines strongly suggestive of trisomy 21 have been found in the Greco-Roman world, in many Central and South American pre-Columbian cultures, and in Khmer temples. 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subjects | Archaeology - history Cambodia Central America Down Syndrome - history Europe History, 15th Century History, 16th Century History, 17th Century History, 18th Century History, 19th Century History, 20th Century History, 21st Century History, Ancient History, Medieval Humans Medicine in the Arts Paintings - history Roman World - history Sculpture - history South America |
title | Trisomy 21 in visual art |
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