Journal of Cystic Fibrosis
Volume 9, Issue 4 , Pages 269-271 , July 2010

Report of two patients with associated conditions in addition to cystic fibrosis

  • Supriya K. Jambhekar

      Affiliations

    • University of Arkansas for Medical Sciences and Arkansas Children's Hospital, 1 Children's Way, # 512-17, Little Rock, AR 72202, USA
    • Corresponding Author InformationCorresponding author. Pulmonary Medicine, University of Arkansas for Medical Sciences, Arkansas Children's Hospital, 1 Children's Way, # 512-17, Little Rock, AR 72202, USA. Tel.: +1 501 364 1006; fax: +1 501 364 3930.
  • ,
  • John L. Carroll

      Affiliations

    • University of Arkansas for Medical Sciences and Arkansas Children's Hospital, 1 Children's Way, # 512-17, Little Rock, AR 72202, USA
  • ,
  • Steven Keiles

      Affiliations

    • Ambry Genetics, 100 Columbia, # 200, Aliso Viejo, CA 92652, USA

Received 29 January 2010 ,Revised 21 April 2010 ,Accepted 22 April 2010.

References 

  1. Rosenstein BJ, Cutting GR. The diagnosis of cystic fibrosis: a consensus statement. J Pediatr. 1998;132:589–595
  2. Hamosh A, FitzSimmons SC, Macek M, Knowles MR, Rosenstein BJ, Cutting GR. Comparison of the clinical manifestations of cystic fibrosis in black and white patients. J Pediatr. 1998;132:255–259
  3. Orenstein D, Rosenstein B, Stern R. In:  Orenstein D,  Rosenstein B,  Stern R editor. Diagnosis of cystic fibrosis. Philadelphia: Lippincott Williams & Wilkins; 2000;
  4. Riordan JR, Rommens JM, Kerem B, Alon N, Roztmahel R, Grzelczak Z, et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science. 1989;245(4922):1066–1073
  5. Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, et al. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science. 1989;245(4922):1059–1065
  6. Cystic fibrosis mutation database statistics. [cited Nov 30, 2009]; Available from: http://www.genet.sickkids.on.ca/cftr/StatisticsPage.html.
  7. Rubinstein JH, Taybi H. Broad thumbs and toes and facial abnormalities. Am J Dis Child. 1963;105:588–608

 Disclosure statement: Co-author Steven Keiles is Vice President, Director of Genetic Services for Ambry Genetics in Aliso Viejo, California, USA.

PII: S1569-1993(10)00064-0

doi: 10.1016/j.jcf.2010.04.007

Journal of Cystic Fibrosis
Volume 9, Issue 4 , Pages 269-271 , July 2010