Scalp skin lesion in Turner syndrome: more than lymphoedema?
Identifieur interne : 007E91 ( Main/Exploration ); précédent : 007E90; suivant : 007E92Scalp skin lesion in Turner syndrome: more than lymphoedema?
Auteurs : A. Debeer [Belgique] ; E. Steenkiste ; K. Devriendt ; M. MorrenSource :
- Clinical dysmorphology [ 0962-8827 ] ; 2005.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Dermatoses du cuir chevelu, Lymphoedème, Syndrome de Turner.
- génétique : Syndrome de Turner.
- étiologie : Dermatoses du cuir chevelu.
- Diagnostic différentiel, Femelle, Humains, Nouveau-né, Syndrome de Turner.
English descriptors
- KwdEn :
- MESH :
- complications : Turner Syndrome.
- etiology : Scalp Dermatoses.
- genetics : Turner Syndrome.
- pathology : Lymphedema, Scalp Dermatoses, Turner Syndrome.
- Diagnosis, Differential, Female, Humans, Infant, Newborn.
Abstract
We present a case of a newborn with Turner syndrome (TS) and a scalp skin lesion resembling cutis verticis gyrata (CVG). Several reports on CVG in TS describe the lesions and correlate it with lymphoedema frequently seen in foetuses and infants with Turner syndrome. Histological examination in this case, however, shows a congenital mucinous nevus. Possibly an abnormal amount of proteoglycans in the skin of patients with TS can clarify the occurrence of this type of skin lesion.
PubMed: 15930906
Affiliations:
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Le document en format XML
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<term>Lymphedema (pathology)</term>
<term>Scalp Dermatoses (etiology)</term>
<term>Scalp Dermatoses (pathology)</term>
<term>Turner Syndrome (complications)</term>
<term>Turner Syndrome (genetics)</term>
<term>Turner Syndrome (pathology)</term>
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<term>Dermatoses du cuir chevelu (étiologie)</term>
<term>Diagnostic différentiel</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphoedème (anatomopathologie)</term>
<term>Nouveau-né</term>
<term>Syndrome de Turner ()</term>
<term>Syndrome de Turner (anatomopathologie)</term>
<term>Syndrome de Turner (génétique)</term>
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<term>Lymphoedème</term>
<term>Syndrome de Turner</term>
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<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Turner Syndrome</term>
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<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Scalp Dermatoses</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Turner Syndrome</term>
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<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Syndrome de Turner</term>
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<term>Turner Syndrome</term>
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<term>Humans</term>
<term>Infant, Newborn</term>
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<term>Humains</term>
<term>Nouveau-né</term>
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<front><div type="abstract" xml:lang="en">We present a case of a newborn with Turner syndrome (TS) and a scalp skin lesion resembling cutis verticis gyrata (CVG). Several reports on CVG in TS describe the lesions and correlate it with lymphoedema frequently seen in foetuses and infants with Turner syndrome. Histological examination in this case, however, shows a congenital mucinous nevus. Possibly an abnormal amount of proteoglycans in the skin of patients with TS can clarify the occurrence of this type of skin lesion.</div>
</front>
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<name sortKey="Morren, M" sort="Morren, M" uniqKey="Morren M" first="M" last="Morren">M. Morren</name>
<name sortKey="Steenkiste, E" sort="Steenkiste, E" uniqKey="Steenkiste E" first="E" last="Steenkiste">E. Steenkiste</name>
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<country name="Belgique"><noRegion><name sortKey="Debeer, A" sort="Debeer, A" uniqKey="Debeer A" first="A" last="Debeer">A. Debeer</name>
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