Healthy growth in children with Down syndrome
To provide cross-sectional height and head circumference (HC) references for healthy Dutch children with Down syndrome (DS), while considering the influence of concomitant disorders on their growth, and to compare growth between children with DS and children from the general population. Longitudinal...
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description | To provide cross-sectional height and head circumference (HC) references for healthy Dutch children with Down syndrome (DS), while considering the influence of concomitant disorders on their growth, and to compare growth between children with DS and children from the general population.
Longitudinal growth and medical data were retrospectively collected from medical records in 25 of the 30 regional hospital-based outpatient clinics for children with DS in The Netherlands. Children with Trisomy 21 karyotype of Dutch descent born after 1982 were included. The LMS method was applied to fit growth references.
We enrolled 1,596 children, and collected 10,558 measurements for height and 1,778 for HC. Children with DS without concomitant disorders (otherwise healthy children) and those suffering only from mild congenital heart defects showed similar growth patterns. The established growth charts, based on all measurements of these two groups, demonstrate the three age periods when height differences between children with and without DS increase: during pregnancy, during the first three years of life, and during puberty. This growth pattern results in a mean final height of 163.4 cm in boys and 151.8 cm in girls (-2.9 standard deviation (SD) and -3.0 SD on general Dutch charts, respectively). Mean HC (0 to 15 months) was 2 SD less than in the general Dutch population. The charts are available at www.tno.nl/growth.
Height and HC references showed that growth retardation in otherwise healthy children with DS meanly occurs in three critical periods of growth, resulting in shorter final stature and smaller HC than the general Dutch population shows. With these references, health care professionals can optimize their preventive care: monitoring growth of individual children with DS optimal, so that growth retarding comorbidities can be identified early, and focusing on the critical age periods to establish ways to optimize growth. |
doi_str_mv | 10.1371/journal.pone.0031079 |
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Longitudinal growth and medical data were retrospectively collected from medical records in 25 of the 30 regional hospital-based outpatient clinics for children with DS in The Netherlands. Children with Trisomy 21 karyotype of Dutch descent born after 1982 were included. The LMS method was applied to fit growth references.
We enrolled 1,596 children, and collected 10,558 measurements for height and 1,778 for HC. Children with DS without concomitant disorders (otherwise healthy children) and those suffering only from mild congenital heart defects showed similar growth patterns. The established growth charts, based on all measurements of these two groups, demonstrate the three age periods when height differences between children with and without DS increase: during pregnancy, during the first three years of life, and during puberty. This growth pattern results in a mean final height of 163.4 cm in boys and 151.8 cm in girls (-2.9 standard deviation (SD) and -3.0 SD on general Dutch charts, respectively). Mean HC (0 to 15 months) was 2 SD less than in the general Dutch population. The charts are available at www.tno.nl/growth.
Height and HC references showed that growth retardation in otherwise healthy children with DS meanly occurs in three critical periods of growth, resulting in shorter final stature and smaller HC than the general Dutch population shows. With these references, health care professionals can optimize their preventive care: monitoring growth of individual children with DS optimal, so that growth retarding comorbidities can be identified early, and focusing on the critical age periods to establish ways to optimize growth.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0031079</identifier><identifier>PMID: 22363551</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adolescent ; Adult ; Age ; Ambulatory care facilities ; Biology ; Body height ; Body Height - physiology ; Body mass index ; Cephalometry ; Charts ; Child ; Child development ; Child, Preschool ; Children ; Children & youth ; Childrens health ; Chromosomes ; Congenital heart defects ; Disabled children ; Disorders ; Down syndrome ; Down Syndrome - physiopathology ; Down's syndrome ; Female ; Girls ; Growth ; Growth and Development ; Growth patterns ; Growth rate ; Health ; Health care ; Heart ; Human growth ; Humans ; Infant ; Infant, Newborn ; Lifestyles ; Male ; Medical records ; Medical referrals ; Medicine ; Netherlands ; Optimization ; Pediatrics ; Physicians ; Population studies ; Pregnancy ; Preventive medicine ; Puberty ; Quality of life ; Reference Standards ; Special education ; Statistics ; Studies ; Trans-Neptunian objects ; Trends ; Trisomy ; Young Adult</subject><ispartof>PloS one, 2012-02, Vol.7 (2), p.e31079-e31079</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Van Gameren-Oosterom et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Van Gameren-Oosterom et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c691t-eed5d696b8aadb184ec702e228efbcbf6d7a64b7accc32f1aa70e4b4b3bd7b3d3</citedby><cites>FETCH-LOGICAL-c691t-eed5d696b8aadb184ec702e228efbcbf6d7a64b7accc32f1aa70e4b4b3bd7b3d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281925/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281925/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79569,79570</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22363551$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Van Gameren-Oosterom, Helma B M</creatorcontrib><creatorcontrib>Van Dommelen, Paula</creatorcontrib><creatorcontrib>Oudesluys-Murphy, Anne Marie</creatorcontrib><creatorcontrib>Buitendijk, Simone E</creatorcontrib><creatorcontrib>Van Buuren, Stef</creatorcontrib><creatorcontrib>Van Wouwe, Jacobus P</creatorcontrib><title>Healthy growth in children with Down syndrome</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>To provide cross-sectional height and head circumference (HC) references for healthy Dutch children with Down syndrome (DS), while considering the influence of concomitant disorders on their growth, and to compare growth between children with DS and children from the general population.
Longitudinal growth and medical data were retrospectively collected from medical records in 25 of the 30 regional hospital-based outpatient clinics for children with DS in The Netherlands. Children with Trisomy 21 karyotype of Dutch descent born after 1982 were included. The LMS method was applied to fit growth references.
We enrolled 1,596 children, and collected 10,558 measurements for height and 1,778 for HC. Children with DS without concomitant disorders (otherwise healthy children) and those suffering only from mild congenital heart defects showed similar growth patterns. The established growth charts, based on all measurements of these two groups, demonstrate the three age periods when height differences between children with and without DS increase: during pregnancy, during the first three years of life, and during puberty. This growth pattern results in a mean final height of 163.4 cm in boys and 151.8 cm in girls (-2.9 standard deviation (SD) and -3.0 SD on general Dutch charts, respectively). Mean HC (0 to 15 months) was 2 SD less than in the general Dutch population. The charts are available at www.tno.nl/growth.
Height and HC references showed that growth retardation in otherwise healthy children with DS meanly occurs in three critical periods of growth, resulting in shorter final stature and smaller HC than the general Dutch population shows. With these references, health care professionals can optimize their preventive care: monitoring growth of individual children with DS optimal, so that growth retarding comorbidities can be identified early, and focusing on the critical age periods to establish ways to optimize growth.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age</subject><subject>Ambulatory care facilities</subject><subject>Biology</subject><subject>Body height</subject><subject>Body Height - physiology</subject><subject>Body mass index</subject><subject>Cephalometry</subject><subject>Charts</subject><subject>Child</subject><subject>Child development</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Children & youth</subject><subject>Childrens health</subject><subject>Chromosomes</subject><subject>Congenital heart defects</subject><subject>Disabled children</subject><subject>Disorders</subject><subject>Down syndrome</subject><subject>Down Syndrome - physiopathology</subject><subject>Down's syndrome</subject><subject>Female</subject><subject>Girls</subject><subject>Growth</subject><subject>Growth and Development</subject><subject>Growth patterns</subject><subject>Growth rate</subject><subject>Health</subject><subject>Health care</subject><subject>Heart</subject><subject>Human growth</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Lifestyles</subject><subject>Male</subject><subject>Medical records</subject><subject>Medical referrals</subject><subject>Medicine</subject><subject>Netherlands</subject><subject>Optimization</subject><subject>Pediatrics</subject><subject>Physicians</subject><subject>Population studies</subject><subject>Pregnancy</subject><subject>Preventive medicine</subject><subject>Puberty</subject><subject>Quality of life</subject><subject>Reference Standards</subject><subject>Special education</subject><subject>Statistics</subject><subject>Studies</subject><subject>Trans-Neptunian objects</subject><subject>Trends</subject><subject>Trisomy</subject><subject>Young 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One</addtitle><date>2012-02-17</date><risdate>2012</risdate><volume>7</volume><issue>2</issue><spage>e31079</spage><epage>e31079</epage><pages>e31079-e31079</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>To provide cross-sectional height and head circumference (HC) references for healthy Dutch children with Down syndrome (DS), while considering the influence of concomitant disorders on their growth, and to compare growth between children with DS and children from the general population.
Longitudinal growth and medical data were retrospectively collected from medical records in 25 of the 30 regional hospital-based outpatient clinics for children with DS in The Netherlands. Children with Trisomy 21 karyotype of Dutch descent born after 1982 were included. The LMS method was applied to fit growth references.
We enrolled 1,596 children, and collected 10,558 measurements for height and 1,778 for HC. Children with DS without concomitant disorders (otherwise healthy children) and those suffering only from mild congenital heart defects showed similar growth patterns. The established growth charts, based on all measurements of these two groups, demonstrate the three age periods when height differences between children with and without DS increase: during pregnancy, during the first three years of life, and during puberty. This growth pattern results in a mean final height of 163.4 cm in boys and 151.8 cm in girls (-2.9 standard deviation (SD) and -3.0 SD on general Dutch charts, respectively). Mean HC (0 to 15 months) was 2 SD less than in the general Dutch population. The charts are available at www.tno.nl/growth.
Height and HC references showed that growth retardation in otherwise healthy children with DS meanly occurs in three critical periods of growth, resulting in shorter final stature and smaller HC than the general Dutch population shows. With these references, health care professionals can optimize their preventive care: monitoring growth of individual children with DS optimal, so that growth retarding comorbidities can be identified early, and focusing on the critical age periods to establish ways to optimize growth.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22363551</pmid><doi>10.1371/journal.pone.0031079</doi><tpages>e31079</tpages><oa>free_for_read</oa></addata></record> |
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source | Public Library of Science (PLoS) Journals Open Access; MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Adolescent Adult Age Ambulatory care facilities Biology Body height Body Height - physiology Body mass index Cephalometry Charts Child Child development Child, Preschool Children Children & youth Childrens health Chromosomes Congenital heart defects Disabled children Disorders Down syndrome Down Syndrome - physiopathology Down's syndrome Female Girls Growth Growth and Development Growth patterns Growth rate Health Health care Heart Human growth Humans Infant Infant, Newborn Lifestyles Male Medical records Medical referrals Medicine Netherlands Optimization Pediatrics Physicians Population studies Pregnancy Preventive medicine Puberty Quality of life Reference Standards Special education Statistics Studies Trans-Neptunian objects Trends Trisomy Young Adult |
title | Healthy growth in children with Down syndrome |
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