Iranian Journal of Pediatrics

Published by: Kowsar

Horseshoe Lung Associated With Holt-Oram Syndrome

Xu Qin 1 , Wang Wei 1 and Gong Fangqi 1 , *
Authors Information
1 Department of Cardiology, Children’s Hospital, Zhejiang University School of Medicine, Hangzhou, China
Article information
  • Iranian Journal of Pediatrics: April 28, 2015, 25 (2); e251
  • Published Online: April 18, 2015
  • Article Type: Letter
  • Received: September 11, 2014
  • Revised: December 22, 2014
  • Accepted: January 10, 2015
  • DOI: 10.5812/ijp.251

To Cite: Qin X, Wei W, Fangqi G. Horseshoe Lung Associated With Holt-Oram Syndrome, Iran J Pediatr. 2015 ;25(2):e251. doi: 10.5812/ijp.251.

Copyright: Copyright © 0, Iranian Journal of Pediatrics. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
References
  • 1. Akay HO, Kervancioglu M, Nazaroglu H, Katar S, Ozmen CA, Kilinc I, et al. Horseshoe lung associated with rare bilateral variant of scimitar syndrome: demonstration by 64-slice MDCT angiography. Pediatr Radiol. 2008; 38(5): 563-6[DOI][PubMed]
  • 2. Basson CT, Solomon SD, Weissman B, MacRae CA, Poznanski AK, Prieto F, et al. Genetic heterogeneity of heart-hand syndromes. Circulation. 1995; 91(5): 1326-9[PubMed]
  • 3. Salerno T, Guccione P, Malena S, Cutrera R. Horseshoe lung associated with unique left pulmonary vein: an unreported association. Pediatr Cardiol. 2010; 31(6): 905-7[DOI][PubMed]
  • 4. Oguz B, Alan S, Ozcelik U, Haliloglu M. Horseshoe lung associated with left-lung hypoplasia, left pulmonary artery sling and bilateral agenesis of upper lobe bronchi. Pediatr Radiol. 2009; 39(9): 1002-5[DOI][PubMed]
  • 5. McDermott DA, Bressan MC, He J, Lee JS, Aftimos S, Brueckner M, et al. TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome. Pediatr Res. 2005; 58(5): 981-6[PubMed]
  • 6. Caglayan AO, Koklu E, Saatci C, Gunes T, Ozkul Y, Narin N, et al. Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2). Ann Saudi Med. 2008; 28(3): 209-12[PubMed]
  • 7. Gonzalez Espinosa C, Artiles Perez L, Garcia Baez M, Otero Gomez A, Garcia Miranda JL. [Holt-Oram syndrome with chromosomopathy (author's transl)]. An Esp Pediatr. 1982; 16(1): 77-81[PubMed]
  • 8. Le Meur N, Goldenberg A, Michel-Adde C, Drouin-Garraud V, Blaysat G, Marret S, et al. Molecular characterization of a 14q deletion in a boy with features of Holt-Oram syndrome. Am J Med Genet A. 2005; 134(4): 439-42[DOI][PubMed]
  • 9. Tseng YR, Su YN, Lu FL, Jeng SF, Hsieh WS, Chen CY, et al. Holt-Oram syndrome with right lung agenesis caused by a de novo mutation in the TBX5 gene. Am J Med Genet A. 2007; 143A(9): 1012-4[DOI][PubMed]
  • 10. Begemann G, Ingham PW. Developmental regulation of Tbx5 in zebrafish embryogenesis. Mech Dev. 2000; 90(2): 299-304[PubMed]
  • 11. Tiozzo C, De Langhe S, Carraro G, Alam DA, Nagy A, Wigfall C, et al. Fibroblast growth factor 10 plays a causative role in the tracheal cartilage defects in a mouse model of Apert syndrome. Pediatr Res. 2009; 66(4): 386-90[DOI][PubMed]
Creative Commons License Except where otherwise noted, this work is licensed under Creative Commons Attribution Non Commercial 4.0 International License .