دورية أكاديمية
MANAGEMENT OF ENDOCRINE DISEASE: Transition of care for young adult patients with Turner syndrome
العنوان: | MANAGEMENT OF ENDOCRINE DISEASE: Transition of care for young adult patients with Turner syndrome |
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المؤلفون: | Bernard V; Service d'Endocrinologie et Maladies de la Reproduction, Centre constitutif du centre de Référence des Maladies Endocriniennes Rares de la Croissance et du Développement (CMERCD), Assistance Publique - Hôpitaux de Paris, Hôpital Saint-Antoine, Paris, France.; Sorbonne Université, F-75012, Paris, France., Donadille B; Service d'Endocrinologie et Maladies de la Reproduction, Centre constitutif du centre de Référence des Maladies Endocriniennes Rares de la Croissance et du Développement (CMERCD), Assistance Publique - Hôpitaux de Paris, Hôpital Saint-Antoine, Paris, France., Le Poulennec T; Service d'Endocrinologie et Maladies de la Reproduction, Centre constitutif du centre de Référence des Maladies Endocriniennes Rares de la Croissance et du Développement (CMERCD), Assistance Publique - Hôpitaux de Paris, Hôpital Saint-Antoine, Paris, France.; Sorbonne Université, F-75012, Paris, France., Nedelcu M; Service d'Endocrinologie et Maladies de la Reproduction, Centre constitutif du centre de Référence des Maladies Endocriniennes Rares de la Croissance et du Développement (CMERCD), Assistance Publique - Hôpitaux de Paris, Hôpital Saint-Antoine, Paris, France., Martinerie L; Service d'Endocrinologie Pédiatrique, Centre de Référence des Maladies Endocriniennes Rares de la Croissance et du Développement (CRMERCD), Hôpital Robert Debré, Assistance Publique - Hôpitaux de Paris, Paris, France.; INSERM Unit 1145, Le Kremlin-Bicêtre, Paris, FranceINSERM UMR_S933, Université Paris Diderot, Sorbonne Paris Cité, Paris, France., Christin-Maitre S; Service d'Endocrinologie et Maladies de la Reproduction, Centre constitutif du centre de Référence des Maladies Endocriniennes Rares de la Croissance et du Développement (CMERCD), Assistance Publique - Hôpitaux de Paris, Hôpital Saint-Antoine, Paris, France.; Sorbonne Université, F-75012, Paris, France.; Sorbonne Université, F-75012, Paris, France. |
المصدر: | European journal of endocrinology [Eur J Endocrinol] 2019 Jan 01; Vol. 180 (1), pp. R1-R7. |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: Oxford University Press Country of Publication: England NLM ID: 9423848 Publication Model: Print Cited Medium: Internet ISSN: 1479-683X (Electronic) Linking ISSN: 08044643 NLM ISO Abbreviation: Eur J Endocrinol Subsets: PubMed not MEDLINE |
أسماء مطبوعة: | Publication: 2023- : Oxford : Oxford University Press Original Publication: Oslo, Norway : Scandinavian University Press, c1994- |
مستخلص: | Turner syndrome (TS), affecting 1/2000 to 1/2500 live born girls, is a chromosomal aberration with a total or partial loss of one of the X chromosomes. The diagnosis can be established from the intra-uterine life to adulthood. TS is a chronic disease with particular morbidity and mortality. The loss to follow-up rate, during transition, between children and adult units, remains a crucial issue. This review focusses on the adolescent and young adult patients with TS. The different goals of TS transition are presented as well as some of the tools available in order to improve this transition. The involvement of the patient’s family, advocacy groups and therapeutic educational programs are discussed. A specificity concerning TS transition, as compared to other chronic diseases, relies on the fact that patients with TS may present a peculiar neurocognitive profile. They are in general more anxious than the general population. Therefore, psychological support should be offered to optimize transition. Data illustrating the beneficial impact of an organised transition of TS, from paediatric units to multidisciplinary adult care systems, within the same reference centre are presented. Further studies are required to evaluate the mid-to-long-term transition of paediatric patients with TS referred to adult units. |
تواريخ الأحداث: | Date Created: 20190223 Date Completed: 20190304 Latest Revision: 20190304 |
رمز التحديث: | 20240628 |
DOI: | 10.1530/EJE-18-0238 |
PMID: | 30793874 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1479-683X |
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DOI: | 10.1530/EJE-18-0238 |