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"Beckwith-Wiedemann" syndrome
- Beckwith-Wiedemann syndrome is a condition that affects many parts of the body. It is classified as an overgrowth syndrome, which means that affected infants ...
- ... on the paternally inherited copy of chromosome 11. Beckwith-Wiedemann syndrome, a condition characterized by overgrowth and other signs ... growth, together lead to overgrowth in people with Beckwith-Wiedemann syndrome.In a few cases, Beckwith-Wiedemann syndrome has ...
- ... structure or number of copies of chromosome 11. Beckwith-Wiedemann syndrome results from the abnormal regulation of genes on ... to overgrowth and the other characteristic features of Beckwith-Wiedemann syndrome.About 20 percent of cases of Beckwith-Wiedemann ...
- ... on the paternally inherited copy of chromosome 11. Beckwith-Wiedemann syndrome, a condition characterized by overgrowth and other signs ... growth, together lead to overgrowth in people with Beckwith-Wiedemann syndrome.In a few cases, Beckwith-Wiedemann syndrome has ...
- ... on the maternally inherited copy of chromosome 11. Beckwith-Wiedemann syndrome is a condition that causes overgrowth and has ... body. At least half of all cases of Beckwith-Wiedemann syndrome result from changes in methylation of the IC2 ...
- ... on the maternally inherited copy of chromosome 11. Beckwith-Wiedemann syndrome is a condition characterized by overgrowth and other ... leads to overgrowth and the other features of Beckwith-Wiedemann syndrome.In a few cases, Beckwith-Wiedemann syndrome has ...
- ... tumor has also been seen in individuals with Beckwith-Wiedemann syndrome, which can be caused by changes in the ...
- ... born with omphalocele have a genetic condition called Beckwith-Wiedemann syndrome. Affected individuals may have additional signs and symptoms ...
- ... with special reference to transient neonatal diabetes and Beckwith-Wiedemann syndrome. Endocr Dev. 2007;12:113-123. doi: 10. ...
- ... with special reference to transient neonatal diabetes and Beckwith-Wiedemann syndrome. Endocr Dev. 2007;12:113-123. doi: 10. ...