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Lymphoscintigraphic manifestations of Hennekam syndrome--a case report.

Identifieur interne : 000227 ( Ncbi/Checkpoint ); précédent : 000226; suivant : 000228

Lymphoscintigraphic manifestations of Hennekam syndrome--a case report.

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

Source :

RBID : pubmed:10609768

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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.

DOI: 10.1177/000331979905001207
PubMed: 10609768


Affiliations:


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pubmed:10609768

Le document en format XML

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<nlm:affiliation>Division of Cardiovascular Medicine, Stanford University School of Medicine, California 94305, USA. rockson@leland.stanford.edu</nlm:affiliation>
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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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