Cardiac disease and Rett syndrome
Rett syndrome (RS) is a neurodevelopmental disease,1 affecting approximately 1 in 10 000–15 000 females.2 Clinical severity of RS may vary with increasing age, following a four stage model.3
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| Veröffentlicht in: | Archives of disease in childhood 2006-05, Vol.91 (5), p.440-443 |
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| container_title | Archives of disease in childhood |
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| creator | Acampa, M Guideri, F |
| description | Rett syndrome (RS) is a neurodevelopmental disease,1 affecting approximately 1 in 10 000–15 000 females.2 Clinical severity of RS may vary with increasing age, following a four stage model.3 |
| doi_str_mv | 10.1136/adc.2005.090290 |
| format | Article |
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Prion diseases ; Development and progression ; Echocardiography ; Female ; General aspects ; Grade 2 ; Heart diseases ; Heart Disorders ; heart rate variability ; HRV ; Humans ; Medical sciences ; Neurology ; QT interval prolongation ; Rett syndrome ; Rett Syndrome - complications ; Rett Syndrome - physiopathology ; Review ; sudden death</subject><ispartof>Archives of disease in childhood, 2006-05, Vol.91 (5), p.440-443</ispartof><rights>Copyright 2006 Archives of Disease in Childhood</rights><rights>2006 INIST-CNRS</rights><rights>Copyright: 2006 Copyright 2006 Archives of Disease in Childhood</rights><rights>Copyright ©2006 BMJ Publishing Group & Royal College of Paediatrics and Child Health</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b560t-2f759bf9a1da742187eb7964075e3a0540c8da025143b84db9fb30904371c9133</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://adc.bmj.com/content/91/5/440.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://adc.bmj.com/content/91/5/440.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,230,313,314,727,780,784,792,885,3196,23571,27922,27924,27925,53791,53793,77600,77631</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17701408$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16632674$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Acampa, M</creatorcontrib><creatorcontrib>Guideri, F</creatorcontrib><title>Cardiac disease and Rett syndrome</title><title>Archives of disease in childhood</title><addtitle>Arch Dis Child</addtitle><description>Rett syndrome (RS) is a neurodevelopmental disease,1 affecting approximately 1 in 10 000–15 000 females.2 Clinical severity of RS may vary with increasing age, following a four stage model.3</description><subject>Adolescent</subject><subject>Adult</subject><subject>Arrhythmias, Cardiac - diagnosis</subject><subject>Arrhythmias, Cardiac - etiology</subject><subject>Arrhythmias, Cardiac - physiopathology</subject><subject>Autonomic Nervous System - physiopathology</subject><subject>Biological and medical sciences</subject><subject>cardiac arrhythmias</subject><subject>Child</subject><subject>Control Groups</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. 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Prion diseases</subject><subject>Development and progression</subject><subject>Echocardiography</subject><subject>Female</subject><subject>General aspects</subject><subject>Grade 2</subject><subject>Heart diseases</subject><subject>Heart Disorders</subject><subject>heart rate variability</subject><subject>HRV</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Neurology</subject><subject>QT interval prolongation</subject><subject>Rett syndrome</subject><subject>Rett Syndrome - complications</subject><subject>Rett Syndrome - physiopathology</subject><subject>Review</subject><subject>sudden death</subject><issn>0003-9888</issn><issn>1468-2044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkc1vEzEQxS0EoiFw5oaCEByQNh1_25dK1YoAolAJAQcu1qzXGzbsR7E3iP73uNqoAS6c5jA_v3nPj5DHFNaUcnWKtV8zALkGC8zCHbKgQpmCgRB3yQIAeGGNMSfkQUo7AMqM4ffJCVWKM6XFgjwtMdYt-lXdpoAprHCoVx_DNK3S9VDHsQ8Pyb0GuxQeHeaSfN68-lS-KS4uX78tzy-KSiqYCtZoaavGIq1RC0aNDpW2SoCWgSNIAd7UCExSwSsj6so2Fc-uBdfUW8r5kpzNulf7qg-1D8MUsXNXse0xXrsRW_f3Zmi_ue340zEwTAudBV4cBOL4Yx_S5Po2-dB1OIRxn5zSObzIB5fk2T_gbtzHIYdz1LAspqVRmSpmaotdcO3gx2EKvyY_dl3YBpezl5fuPH-3olRymfnTmfdxTCmG5tY6BXdTlstluZuy3FxWfvHkz8RH_tBOBp4fAEweuybi4Nt05LQGKsAcrbYpW7zdY_yeQ3Mt3YcvpVPv7OYre6_dJvMvZ77qd_91-Rs10rT5</recordid><startdate>20060501</startdate><enddate>20060501</enddate><creator>Acampa, M</creator><creator>Guideri, F</creator><general>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</general><general>BMJ</general><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><general>BMJ Group</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0-V</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88B</scope><scope>88E</scope><scope>88I</scope><scope>8A4</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20060501</creationdate><title>Cardiac disease and Rett syndrome</title><author>Acampa, M ; Guideri, F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b560t-2f759bf9a1da742187eb7964075e3a0540c8da025143b84db9fb30904371c9133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Arrhythmias, Cardiac - diagnosis</topic><topic>Arrhythmias, Cardiac - etiology</topic><topic>Arrhythmias, Cardiac - physiopathology</topic><topic>Autonomic Nervous System - physiopathology</topic><topic>Biological and medical sciences</topic><topic>cardiac arrhythmias</topic><topic>Child</topic><topic>Control Groups</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. 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| subjects | Adolescent Adult Arrhythmias, Cardiac - diagnosis Arrhythmias, Cardiac - etiology Arrhythmias, Cardiac - physiopathology Autonomic Nervous System - physiopathology Biological and medical sciences cardiac arrhythmias Child Control Groups Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Development and progression Echocardiography Female General aspects Grade 2 Heart diseases Heart Disorders heart rate variability HRV Humans Medical sciences Neurology QT interval prolongation Rett syndrome Rett Syndrome - complications Rett Syndrome - physiopathology Review sudden death |
| title | Cardiac disease and Rett syndrome |
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