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Lymphoscintigraphic Manifestations of Hennekam Syndrome

Identifieur interne : 004319 ( Istex/Curation ); précédent : 004318; suivant : 004320

Lymphoscintigraphic Manifestations of Hennekam Syndrome

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

Source :

RBID : ISTEX:8E775379B5FB9F1821759B7F502644E36837EC7C

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:
DOI: 10.1177/000331979905001207

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ISTEX:8E775379B5FB9F1821759B7F502644E36837EC7C

Le document en format XML

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<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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