> Details

Draaken, Markus; Baudisch, Friederike; Timmermann, Bernd; Kuhl, Heiner; Kerick, Martin; Proske, Judith; Wittler, Lars; Pennimpede, Tracie; Ebert, Anne‐Karoline; Rösch, Wolfgang; Stein, Raimund; Bartels, Enrika; von Lowtzow, Catharina; Boemers, Thomas M.; Herms, Stefan; Gearhart, John P.; Lakshmanan, Yegappan; Kockum, Christina Clementsson; Holmdahl, Gundela; Läckgren, Göran; Nordenskjöld, Agnetha; Boyadjiev, Simeon A.; Herrmann, Bernhard G.; Nöthen, Markus M.; [...]

Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region

Reference
management

Bookmarks

Remove from
bookmarks

Share this on Whatsapp

Close

Bookmarks



You can manage bookmarks using lists, please log in to your user account for this.
  • Media type: E-Article
  • Title: Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region
  • Contributor: Draaken, Markus; Baudisch, Friederike; Timmermann, Bernd; Kuhl, Heiner; Kerick, Martin; Proske, Judith; Wittler, Lars; Pennimpede, Tracie; Ebert, Anne‐Karoline; Rösch, Wolfgang; Stein, Raimund; Bartels, Enrika; von Lowtzow, Catharina; Boemers, Thomas M.; Herms, Stefan; Gearhart, John P.; Lakshmanan, Yegappan; Kockum, Christina Clementsson; Holmdahl, Gundela; Läckgren, Göran; Nordenskjöld, Agnetha; Boyadjiev, Simeon A.; Herrmann, Bernhard G.; Nöthen, Markus M.; [...]
  • Published: Wiley, 2014
  • Published in: Birth Defects Research Part A: Clinical and Molecular Teratology, 100 (2014) 6, Seite 512-517
  • Language: English
  • DOI: 10.1002/bdra.23249
  • ISSN: 1542-0752; 1542-0760
  • Keywords: Developmental Biology ; Embryology ; General Medicine ; Pediatrics, Perinatology and Child Health
  • Origination:
  • Footnote:
  • Description: <jats:sec><jats:title>Background</jats:title><jats:p>Classic bladder exstrophy (CBE) is the most common form of the bladder exstrophy and epispadias complex. Previously, we and others have identified four patients with a duplication of 22q11.21 among a total of 96 unrelated CBE patients.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Here, we investigated whether this chromosomal aberration was commonly associated with CBE/bladder exstrophy and epispadias complex in an extended case‐control sample. Multiplex ligation‐dependent probe amplification and microarray‐based analysis were used to identify 22q11.21 duplications in 244 unrelated bladder exstrophy and epispadias complex patients (including 217 CBE patients) and 665 healthy controls.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>New duplications of variable size were identified in four CBE patients and one control. Pooling of our previous and present data (eight duplications in 313 CBE patients) yielded a combined odds ratio of 31.86 (95% confidence interval, 4.24–1407.97). Array‐based sequence capture and high‐throughput targeted re‐sequencing established that all breakpoints resided within the low‐copy repeats 22A to 22D. Comparison of the eight duplications revealed a 414 kb phenocritical region harboring 12 validated RefSeq genes. Characterization of these 12 candidate genes through whole‐mount in situ hybridization of mouse embryos at embryonic day 9.5 suggested that <jats:italic>CRKL</jats:italic>, <jats:italic>THAP7</jats:italic>, and <jats:italic>LZTR1</jats:italic> are CBE candidate genes.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Our data suggest that duplication of 22q11.21 increases CBE risk and implicate a phenocritical region in disease formation. <jats:italic>Birth Defects Research (Part A) 100:512–517, 2014</jats:italic>. © 2014 Wiley Periodicals, Inc.</jats:p></jats:sec>