DESCRIBING LYMPHEDEMA IN FEMALES WITH TURNER SYNDROME.
Identifieur interne : 001F33 ( Main/Exploration ); précédent : 001F32; suivant : 001F34DESCRIBING LYMPHEDEMA IN FEMALES WITH TURNER SYNDROME.
Auteurs : J. Rothbauer ; S. Driver ; L. CallenderSource :
- Lymphology [ 0024-7766 ] ; 2015.
Descripteurs français
- KwdFr :
- MESH :
- diagnostic : Lymphoedème.
- psychologie : Lymphoedème.
- épidémiologie : Lymphoedème.
- Adolescent, Adulte, Adulte d'âge moyen, Enfant, Enquêtes et questionnaires, Facteurs de l'âge, Femelle, Humains, Jeune adulte, Syndrome de Turner, Études transversales.
English descriptors
- KwdEn :
- MESH :
- complications : Turner Syndrome.
- diagnosis : Lymphedema.
- epidemiology : Lymphedema.
- psychology : Lymphedema.
- Adolescent, Adult, Age Factors, Child, Cross-Sectional Studies, Female, Humans, Middle Aged, Surveys and Questionnaires, Young Adult.
Abstract
Turner syndrome (TS) is a chromosomal condition affecting an estimated 1 in 2,500 girls where the second X chromosome is missing, or partially formed. This abnormality affects multiple body systems and can lead to short stature, cardiac, neural, and renal abnormalities. Due to the chronic, non-life threatening nature of lymphedema in comparison to other symptoms of TS, it is often ignored by girls and women with TS and their physicians. Consequently, little is known about how lymphedema affects girls and women with TS across the lifespan. Therefore, the objective of the study was to deliver an online survey for females with TS and caregivers in the US, UK, and Canada to provide a worldwide perspective on their current experience with lymphedema within the spectrum of TS. There were 219 participants who completed the survey, and we were able to identify incidence and characteristics of lymphedema across the lifespan. In addition, we found that females with 45,X karyotyping were more likely to report lymphedema symptoms. Lymphedema is not the most significant concern of females with TS, but education, physician evaluation, and assistance with referrals for treatment and management would improve the ease of managing lymphedema in girls and women with TS.
PubMed: 26939161
Affiliations:
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Le document en format XML
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<term>Female</term>
<term>Humans</term>
<term>Lymphedema (diagnosis)</term>
<term>Lymphedema (epidemiology)</term>
<term>Lymphedema (psychology)</term>
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<term>Femelle</term>
<term>Humains</term>
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<term>Lymphoedème (psychologie)</term>
<term>Lymphoedème (épidémiologie)</term>
<term>Syndrome de Turner ()</term>
<term>Études transversales</term>
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<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Lymphoedème</term>
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<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Lymphedema</term>
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<keywords scheme="MESH" qualifier="psychologie" xml:lang="fr"><term>Lymphoedème</term>
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<keywords scheme="MESH" qualifier="psychology" xml:lang="en"><term>Lymphedema</term>
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<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr"><term>Lymphoedème</term>
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<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Age Factors</term>
<term>Child</term>
<term>Cross-Sectional Studies</term>
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<term>Humans</term>
<term>Middle Aged</term>
<term>Surveys and Questionnaires</term>
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<term>Enfant</term>
<term>Enquêtes et questionnaires</term>
<term>Facteurs de l'âge</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Syndrome de Turner</term>
<term>Études transversales</term>
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<front><div type="abstract" xml:lang="en">Turner syndrome (TS) is a chromosomal condition affecting an estimated 1 in 2,500 girls where the second X chromosome is missing, or partially formed. This abnormality affects multiple body systems and can lead to short stature, cardiac, neural, and renal abnormalities. Due to the chronic, non-life threatening nature of lymphedema in comparison to other symptoms of TS, it is often ignored by girls and women with TS and their physicians. Consequently, little is known about how lymphedema affects girls and women with TS across the lifespan. Therefore, the objective of the study was to deliver an online survey for females with TS and caregivers in the US, UK, and Canada to provide a worldwide perspective on their current experience with lymphedema within the spectrum of TS. There were 219 participants who completed the survey, and we were able to identify incidence and characteristics of lymphedema across the lifespan. In addition, we found that females with 45,X karyotyping were more likely to report lymphedema symptoms. Lymphedema is not the most significant concern of females with TS, but education, physician evaluation, and assistance with referrals for treatment and management would improve the ease of managing lymphedema in girls and women with TS.</div>
</front>
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