LymphedemaV1, Main, Curation, bibRecord, 00AD90

Lymphoscintigraphic Manifestations of Hennekam Syndrome

Identifieur interne : 00AD90 ( Main/Curation ); précédent : 00AD89; suivant : 00AD91

Lymphoscintigraphic Manifestations of Hennekam Syndrome

Auteurs : Stanley G. Rockson ; Maribeth De Los Santos ; Andrzej Szuba ; Stanley G. Rockson [États-Unis]

Source :

Angiology [ 0003-3197 ] ; 1999-12.

RBID : ISTEX:8E775379B5FB9F1821759B7F502644E36837EC7C

Descripteurs français

KwdFr :
- Adolescent, Déficience intellectuelle, Faciès, Femelle, Humains, Lymphangiectasie intestinale (imagerie diagnostique), Lymphoedème (imagerie diagnostique), Scintigraphie, Syndrome.
MESH :
- imagerie diagnostique : Lymphangiectasie intestinale, Lymphoedème.
- Adolescent, Déficience intellectuelle, Faciès, Femelle, Humains, Scintigraphie, Syndrome.
Pascal (Inist)
- Arriération mentale, Congénital, Etude cas, Forme clinique, Homme, Lymphatique, Lymphoedème, Scintigraphie.
Wicri :
- topic : Homme.

English descriptors

KwdEn :
- Adolescent, Case study, Clinical form, Congenital, Facies, Female, Human, Humans, Intellectual Disability, Lymphangiectasis, Intestinal (diagnostic imaging), Lymphatic, Lymphedema, Lymphedema (diagnostic imaging), Mental retardation, Radionuclide Imaging, Scintigraphy, Syndrome.
MESH :
- diagnostic imaging : Lymphangiectasis, Intestinal, Lymphedema.
- Adolescent, Facies, Female, Humans, Intellectual Disability, Radionuclide Imaging, Syndrome.

Abstract

Hennekam syndrome is a rare, recently described genetic disorder in which facial anomalies and mental retardation accompany congenital lymphedema and intestinal lymphangiectasia. Several other somatic abnormalities have variously been described, as have milder degrees of lymphatic dysfunction. The authors herein describe a case of Hennekam syndrome in which the diagnostic difficulties were partially overcome by the judicious use of radionuclide scintigraphy to verify the lymphedematous component of the patient's presentation.

Url:

https://api.istex.fr/document/8E775379B5FB9F1821759B7F502644E36837EC7C/fulltext/pdf

DOI: 10.1177/000331979905001207

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ISTEX:8E775379B5FB9F1821759B7F502644E36837EC7C

Le document en format XML

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<front><div type="abstract" xml:lang="en">Hennekam syndrome is a rare, recently described genetic disorder in which facial anomalies and mental retardation accompany congenital lymphedema and intestinal lymphangiectasia. Several other somatic abnormalities have variously been described, as have milder degrees of lymphatic dysfunction. The authors herein describe a case of Hennekam syndrome in which the diagnostic difficulties were partially overcome by the judicious use of radionuclide scintigraphy to verify the lymphedematous component of the patient's presentation.</div>
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<front><div type="abstract" xml:lang="en">Hennekam syndrome is a rare, recently described genetic disorder in which facial anomalies and mental retardation accompany congenital lymphedema and intestinal lymphangiectasia. Several other somatic abnormalities have variously been described, as have milder degrees of lymphatic dysfunction. The authors herein describe a case of Hennekam syndrome in which the diagnostic difficulties were partially overcome by the judicious use of radionuclide scintigraphy to verify the lymphedematous component of the patient's presentation.</div>
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<idno type="ISSN">0003-3197</idno>
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<idno type="istex">8E775379B5FB9F1821759B7F502644E36837EC7C</idno>
<idno type="DOI">10.1177/000331979905001207</idno>
<idno type="ArticleID">10.1177_000331979905001207</idno>
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<seriesStmt><idno type="ISSN">0003-3197</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Facies</term>
<term>Female</term>
<term>Humans</term>
<term>Intellectual Disability</term>
<term>Lymphangiectasis, Intestinal (diagnostic imaging)</term>
<term>Lymphedema (diagnostic imaging)</term>
<term>Radionuclide Imaging</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adolescent</term>
<term>Déficience intellectuelle</term>
<term>Faciès</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphangiectasie intestinale (imagerie diagnostique)</term>
<term>Lymphoedème (imagerie diagnostique)</term>
<term>Scintigraphie</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Lymphangiectasis, Intestinal</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr"><term>Lymphangiectasie intestinale</term>
<term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Facies</term>
<term>Female</term>
<term>Humans</term>
<term>Intellectual Disability</term>
<term>Radionuclide Imaging</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term>
<term>Déficience intellectuelle</term>
<term>Faciès</term>
<term>Femelle</term>
<term>Humains</term>
<term>Scintigraphie</term>
<term>Syndrome</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
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<front><div type="abstract" xml:lang="en">Hennekam syndrome is a rare, recently described genetic disorder in which facial anomalies and mental retardation accompany congenital lymphedema and intestinal lymphangiectasia. Several other somatic abnormalities have variously been described, as have milder degrees of lymphatic dysfunction. The authors herein describe a case of Hennekam syndrome in which the diagnostic difficulties were partially overcome by the judicious use of radionuclide scintigraphy to verify the lymphedematous component of the patient's presentation.</div>
</front>
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Lymphoscintigraphic Manifestations of Hennekam Syndrome

Lymphoscintigraphic Manifestations of Hennekam Syndrome

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