LymphedemaV1, PascalFrancis, Curation, bibRecord, 000003

Lymphoscintigraphic manifestations of Hennekam syndrome : A case report

Identifieur interne : 000003 ( PascalFrancis/Curation ); précédent : 000002; suivant : 000004

Lymphoscintigraphic manifestations of Hennekam syndrome : A case report

Auteurs : S. G. Rockson [États-Unis] ; M. De Los Santos [États-Unis] ; A. Szuba [États-Unis]

Source :

Angiology [ 0003-3197 ] ; 1999.

RBID : Pascal:00-0034778

Descripteurs français

Pascal (Inist)
- Lymphoedème, Congénital, Scintigraphie, Lymphatique, Arriération mentale, Forme clinique, Homme, Etude cas.
Wicri :
- topic : Homme.

English descriptors

KwdEn :
- Case study, Clinical form, Congenital, Human, Lymphatic, Lymphedema, Mental retardation, Scintigraphy.

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.

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C01	`01`		`ENG`	@0 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.
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C07	`01`	`X`	`SPA`	`@0 Aparato circulatorio patología @5 37`
C07	`02`	`X`	`FRE`	`@0 Lymphatique pathologie @5 38`
C07	`02`	`X`	`ENG`	`@0 Lymphatic vessel disease @5 38`
C07	`02`	`X`	`SPA`	`@0 Linfático patología @5 38`
C07	`03`	`X`	`FRE`	`@0 Exploration radioisotopique @5 45`
C07	`03`	`X`	`ENG`	`@0 Radionuclide study @5 45`
C07	`03`	`X`	`SPA`	`@0 Exploración radioisotópica @5 45`
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C07	`04`	`X`	`SPA`	`@0 Imageneria medical @5 46`
N21				`@1 024`

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Pascal:00-0034778

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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Lymphoscintigraphic manifestations of Hennekam syndrome : A case report

Lymphoscintigraphic manifestations of Hennekam syndrome : A case report

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

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