Lymphoscintigraphic manifestations of Hennekam syndrome : A case report
Identifieur interne : 000957 ( PascalFrancis/Corpus ); précédent : 000956; suivant : 000958Lymphoscintigraphic manifestations of Hennekam syndrome : A case report
Auteurs : S. G. Rockson ; M. De Los Santos ; A. SzubaSource :
- Angiology [ 0003-3197 ] ; 1999.
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- Pascal (Inist)
English descriptors
- KwdEn :
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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Format Inist (serveur)
NO : | PASCAL 00-0034778 INIST |
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ET : | Lymphoscintigraphic manifestations of Hennekam syndrome : A case report |
AU : | ROCKSON (S. G.); DE LOS SANTOS (M.); SZUBA (A.) |
AF : | Division of Cardiovascular Medicine, Stanford University School of Medicine/Stanford, California/Etats-Unis (1 aut., 2 aut., 3 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | Angiology; ISSN 0003-3197; Coden ANGIAB; Etats-Unis; Da. 1999; Vol. 50; No. 12; Pp. 1017-1020; Bibl. 22 ref. |
LA : | Anglais |
EA : | 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. |
CC : | 002B12B04 |
FD : | Lymphoedème; Congénital; Scintigraphie; Lymphatique; Arriération mentale; Forme clinique; Homme; Etude cas |
FG : | Appareil circulatoire pathologie; Lymphatique pathologie; Exploration radioisotopique; Imagerie médicale |
ED : | Lymphedema; Congenital; Scintigraphy; Lymphatic; Mental retardation; Clinical form; Human; Case study |
EG : | Cardiovascular disease; Lymphatic vessel disease; Radionuclide study; Medical imagery |
SD : | Linfedema; Congénito; Centelleografía; Linfático; Retraso mental; Forma clínica; Hombre; Estudio caso |
LO : | INIST-8327.354000080835120070 |
ID : | 00-0034778 |
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Pascal:00-0034778Le 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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<ET>Lymphoscintigraphic manifestations of Hennekam syndrome : A case report</ET>
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<EA>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.</EA>
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