Turner's syndrome in dermatology.
Identifieur interne : 004024 ( PubMed/Curation ); précédent : 004023; suivant : 004025Turner's syndrome in dermatology.
Auteurs : Eve J. Lowenstein [États-Unis] ; Karen H. Kim ; Sharon A. GlickSource :
- Journal of the American Academy of Dermatology [ 0190-9622 ] ; 2004.
Descripteurs français
- KwdFr :
- MESH :
- diagnostic : Syndrome de Turner.
- génétique : Syndrome de Turner.
- Chéloïde, Femelle, Humains, Lymphoedème, Maladies de la peau, Naevus, Syndrome de Turner, Tumeurs cutanées.
English descriptors
- KwdEn :
- MESH :
- complications : Keloid, Lymphedema, Nevus, Skin Diseases, Skin Neoplasms, Turner Syndrome.
- diagnosis : Turner Syndrome.
- genetics : Turner Syndrome.
- therapy : Lymphedema, Skin Diseases.
- Female, Humans.
Abstract
Turner's syndrome (TS) is a common genetic disorder of girls and women, for which the defining clinical triad is short stature, impaired sexual development, and infertility. Although classically known as monosomy X, genetic heterogeneity is frequent in TS, with mosaicism conferring a survival advantage. Several genetic loci have been implicated in TS including the short stature homeobox gene. TS effects many organs, with cutaneous stigmata providing critical clues for early detection of TS. The presence of lymphedema and its cutaneous sequelae are predictive of other systemic disorders, such as cardiac disease. Although an increased number of benign nevi have been reported in TS, the decreased melanoma rate in this population suggests some protective factor is active. Keloids were thought to be prevalent in TS, but recent data suggest otherwise. Autoimmune diseases are common in TS, with a possible increased prevalence of alopecia areata and vitiligo. The following review discusses new insights into the genetics and pathogenesis of this complex disorder, summarizes the major systemic effects, and reviews skin manifestations of TS and their implications.
DOI: 10.1016/j.jaad.2003.07.031
PubMed: 15097963
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pubmed:15097963Le document en format XML
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<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Dermatology, State University New York Health Science Center at Brooklyn, Brooklyn, New York 11203</wicri:regionArea>
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<author><name sortKey="Kim, Karen H" sort="Kim, Karen H" uniqKey="Kim K" first="Karen H" last="Kim">Karen H. Kim</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Female</term>
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<term>Lymphedema (therapy)</term>
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<term>Lymphoedème ()</term>
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<term>Naevus ()</term>
<term>Syndrome de Turner ()</term>
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<term>Lymphoedème</term>
<term>Maladies de la peau</term>
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<front><div type="abstract" xml:lang="en">Turner's syndrome (TS) is a common genetic disorder of girls and women, for which the defining clinical triad is short stature, impaired sexual development, and infertility. Although classically known as monosomy X, genetic heterogeneity is frequent in TS, with mosaicism conferring a survival advantage. Several genetic loci have been implicated in TS including the short stature homeobox gene. TS effects many organs, with cutaneous stigmata providing critical clues for early detection of TS. The presence of lymphedema and its cutaneous sequelae are predictive of other systemic disorders, such as cardiac disease. Although an increased number of benign nevi have been reported in TS, the decreased melanoma rate in this population suggests some protective factor is active. Keloids were thought to be prevalent in TS, but recent data suggest otherwise. Autoimmune diseases are common in TS, with a possible increased prevalence of alopecia areata and vitiligo. The following review discusses new insights into the genetics and pathogenesis of this complex disorder, summarizes the major systemic effects, and reviews skin manifestations of TS and their implications.</div>
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<Abstract><AbstractText>Turner's syndrome (TS) is a common genetic disorder of girls and women, for which the defining clinical triad is short stature, impaired sexual development, and infertility. Although classically known as monosomy X, genetic heterogeneity is frequent in TS, with mosaicism conferring a survival advantage. Several genetic loci have been implicated in TS including the short stature homeobox gene. TS effects many organs, with cutaneous stigmata providing critical clues for early detection of TS. The presence of lymphedema and its cutaneous sequelae are predictive of other systemic disorders, such as cardiac disease. Although an increased number of benign nevi have been reported in TS, the decreased melanoma rate in this population suggests some protective factor is active. Keloids were thought to be prevalent in TS, but recent data suggest otherwise. Autoimmune diseases are common in TS, with a possible increased prevalence of alopecia areata and vitiligo. The following review discusses new insights into the genetics and pathogenesis of this complex disorder, summarizes the major systemic effects, and reviews skin manifestations of TS and their implications.</AbstractText>
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