Beckwith-Wiedemann syndrome
- Beckwith-Wiedemann syndrome
Beck·with-Wie·de·mann syndrome 'bek-wəth-'wēd-ə-mən-, -.man- n an inherited disease that is characterized by macroglossia, umbilical hernia, hypoglycemia, abnormal enlargement of the viscera, and increased risk of Wilms' tumor and rhabdomyosarcoma
Beckwith John Bruce (b 1933)
American pathologist. Beckwith held positions as professor of pathology and pediatrics at the University of Washington's Medical School and chairman of the department of pathology at Children's Hospital in Denver. His areas of research included sudden death during infancy and pathogenesis of tumors in children. He described the syndrome which now bears his name as well as Wiedemann's in an article published independently of Wiedemann in 1964.
Wie·de·mann 'vē-də-.män Hans Rudolf (b 1915)
German pediatrician. In the course of his career Wiedemann served as director of children's clinics in Bonn, Krefeld, and Kiel and on the medical faculty at the universities of Bonn and Kiel. He published several articles on congenital malformations, including the first report on the effects of thalidomide, and on hereditary diseases of the skeleton and nervous system. In 1964 he published an independent description of the syndrome that now bears his name as well as Beckwith's.
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Beck·with-Wie·de·mann syndrome (bekґwith veґdə-mahn) [J.B. Beckwith; Hans Rudolf Wiedemann, German pediatrician, 1915–2006] see under syndrome.
Medical dictionary.
2011.
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Beckwith-Wiedemann syndrome — Infobox Disease Name = Beckwith Wiedemann syndrome Caption = DiseasesDB = 14141 ICD10 = ICD10|Q|87|3|q|80 ICD9 = ICDO = OMIM = 130650 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 218 MeshName = Beckwith Wiedemann+Syndrome MeshNumber =… … Wikipedia
Beckwith-Wiedemann syndrome — A rare, overgrowth disorder in which babies are large at birth and may develop low blood sugar. Other common symptoms are a large tongue, large internal organs, and defects of the abdominal wall near the navel. Beckwith Wiedemann syndrome… … English dictionary of cancer terms
Beckwith-Wiedemann syndrome — Rare developmental disorder with a complex pattern of inheritance suggesting a defect in maternal imprinting. Characteristics are all growth abnormalities enlarged tongue, gigantism, enlarged adrenal glands, enlarged visceral organs, advanced… … Dictionary of molecular biology
Beckwith-Wiedemann syndrome — noun A congenital overgrowth disorder characterized by an increased risk of childhood cancer and certain physical defects. Syn: BWS … Wiktionary
Syndrome de beckwith-wiedemann — CIM 10 : Q87.3 Le syndrome de Beckwith Wiedemann est une maladie génétique se caractérisant par une croissance excessive du fœtus, une grosse langue (macroglossie), une hypertrophie des organes, une omphalocèle ou une hernie, une prédisposition à … Wikipédia en Français
Beckwith-Wiedemann-Syndrom — Klassifikation nach ICD 10 Q87.3 Angeborene Fehlbildungssyndrome mit vermehrtem Gewebewachstum im frühen Kindesalter Wiedemann Beckwith Syndrom … Deutsch Wikipedia
Syndrome de Beckwith-Wiedemann — Classification internationale des maladies CIM 10 : Q87.3 Le syndrome de Beckwith Wiedemann est une maladie génétique se caractérisant par une croissance excessive du fœtus, une grosse langue (macroglossie), une hypertrophie des organes, une… … Wikipédia en Français
Síndrome de Beckwith Wiedemann — Clasificación y recursos externos CIE 10 Q 87.3, q 80 OMIM 130650 DiseasesDB … Wikipedia Español
Syndrome de Beckwith-Wideman — Syndrome de Beckwith Wiedemann Syndrome de Beckwith Wiedemann CIM 10 : Q87.3 Le syndrome de Beckwith Wiedemann est une maladie génétique se caractérisant par une croissance excessive du fœtus, une grosse langue (macroglossie), une hypertrophie… … Wikipédia en Français
Syndrôme de Beckwith-Wideman — Syndrome de Beckwith Wiedemann Syndrome de Beckwith Wiedemann CIM 10 : Q87.3 Le syndrome de Beckwith Wiedemann est une maladie génétique se caractérisant par une croissance excessive du fœtus, une grosse langue (macroglossie), une hypertrophie… … Wikipédia en Français