Beckwith-Wiedemann Syndrome is a genetic growth disorder that is usually present at birth. It is characterized by low blood sugar at birth, abdominal organs that stick out of the belly button, and a higher likelihood of tumors or cancers. The symptoms of Beckwith-Wiedemann Syndrome include enlarged organs, prominent eyes, and seizures. Treatment for Beckwith-Wiedemann Syndrome usually includes surgical repair of the abdominal organs and treatment of the blood sugar. Once the person has survived childhood, the outlook is good, but tumors are still likely.
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We have 1574 products for the study of Beckwith-wiedemann Syndrome that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Beckwith-wiedemann Syndrome is also known as beckwith-wiedemann syndrome, wiedemann-beckwith syndrome (wbs), emg syndrome, exomphalos macroglossia gigantism syndrome, exomphalos-macroglossia-gigantism syndrome.