Genetics, diagnosis and characteristics of trisomy 21
Copyright © 2018 Elsevier Masson SAS. All rights reserved..
Trisomy 21 remains relevant today. As patients' life expectancy increases, medical monitoring shows the importance of screening for associated complications such as epilepsy and sleep apnoea. For caregivers, it constitutes a care model for intellectually disabled people notably with regard to anxiety, poor expression of pain and family suffering. Scientific advances raise hope of progress in therapeutic practices.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2018 |
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| Erschienen: |
2018 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:39 |
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| Enthalten in: |
Soins. Pediatrie, puericulture - 39(2018), 302 vom: 01. Mai, Seite 10-14 |
| Sprache: |
Französisch |
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| Weiterer Titel: |
Génétique, diagnostic et caractéristiques de la trisomie 21 |
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| Beteiligte Personen: |
Ravel, Aimé [VerfasserIn] |
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| Links: |
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| Themen: |
Amniocentèse |
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| Anmerkungen: |
Date Completed 08.11.2018 Date Revised 08.11.2018 published: Print Citation Status MEDLINE |
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| doi: |
10.1016/j.spp.2018.03.002 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM283945494 |
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| 520 | |a Trisomy 21 remains relevant today. As patients' life expectancy increases, medical monitoring shows the importance of screening for associated complications such as epilepsy and sleep apnoea. For caregivers, it constitutes a care model for intellectually disabled people notably with regard to anxiety, poor expression of pain and family suffering. Scientific advances raise hope of progress in therapeutic practices | ||
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| 650 | 4 | |a trisomy 21 | |
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