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Lymphoscintigraphic manifestations of Hennekam syndrome : A case report

Identifieur interne : 000981 ( PascalFrancis/Checkpoint ); précédent : 000980; suivant : 000982

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 :

RBID : Pascal:00-0034778

Descripteurs français

English descriptors

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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Pascal:00-0034778

Le document en format XML

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{{Explor lien
   |wiki=    Wicri/Sante
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   |texte=   Lymphoscintigraphic manifestations of Hennekam syndrome : A case report
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