147
Views
0
CrossRef citations to date
0
Altmetric
Case Report

RETICULAR DYSGENESIS IN A PRETERM INFANT: A Case Report

, MD, , MD, , MD, , MD, , MD, , MD, , MD, , MD & , MD show all
Pages 646-649 | Received 23 Jun 2010, Accepted 13 Jul 2010, Published online: 23 Sep 2010

REFERENCES

  • Rosen FS, Wedgwood RJD, Eibl M Primary immunodeficiency diseases. Clin Exp Immunol. 1995;99:1–24.
  • de Vaal OM, Seynhaeve V. Reticular dysgenesia. Lancet. 1959;19:1123–1125.
  • Barjaktarevic I, Maletkovic-Barjaktarevic J, Kamani NR, Vukmanovic S. Altered functional balance of Gf-1 and Gf-1b as an alternative cause of reticular dysgenesis? Med Hypotheses. 2010;74:445–448.
  • Ownby DR, Pizzo S, Blackmon L Severe combined immunodeficiency with leukopenia (reticular dysgenesis) in siblings: immunologic and histopathologic findings. J Pediatr. 1976;89:382–387.
  • Alonso K, Dew JM, Starke WR. Thymic alymphoplasia and congenital aleukocytosis (reticular dysgenesia). Arch Pathol. 1972;94:179–183.
  • Haas RJ, Niethammer D, Goldmann SF Congenital immunodeficiency and agranulocytosis (reticular dysgenesia). Act Paediatr Scand. 1977;66:279–283.
  • De La Calle-Martin O, Badell I, Garcia A B cells and monocytes are not developmentally affected in a case of reticular dysgenesis. Clin Exp Immunol. 1997;110:392–396.
  • Friedrich W, Goldmann SF, Ebell W Severe combined immunodeficiency: treatment by bone marrow transplantation in 15 infants using HLA-haploidentical donors. Eur J Pediatr. 1985;144: 125–130.
  • Heymer B, Friedrich W, Knobloch C, Goldmann SF. Reticular dysgenesis: primary disorder in differentiation of hematopoietic stem cells? Verh Dtsch Ges Pathol. 1990;74:106–110.
  • Espanol T, Compte J, Alvarez C Reticular dysgenesis: report of two brothers. Clin Exp Immunol. 1979;38:615–620.
  • Bujan W, Ferster A, Sariban E, Friedrich W. Effect of recombinant human granulocyte colony-stimulating factor in reticular dysgenesis. Blood. 1993;82:1684.
  • Pannicke U, Honig M, Hess I Reticular dysgenesis (aleukocytosis) is caused by mutations in the gene encoding mitochondrial adenylate kinase 2. Nat Genet. 2009;41:101–105.
  • Lagresle-Peyrou C, Six EM, Picard C Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness. Nat Genet. 2009;41:106–111.
  • Small TN, Wall DA, Kurtzberg J Association of reticular dysgenesis (thymic alymphoplasia and congenital aleukocytosis) with bilateral sensorineural deafness. J Pediatr. 1999;135:387–389.
  • Bertrand Y, Muller SM, Casanova JL Reticular dysgenesis: HLA non-identical bone marrow transplants in a series of 10 patients. Bone Marrow Transplant. 2002;29:759–762.
  • Heltzer ML, Paessler M, Raffini L Successful haploidentical bone marrow transplantation in a patient with reticular dysgenesis: three-year follow-up. J Allergy Clin Immunol. 2007;120:950–952.
  • Reubsaet LL, Boelens JJ, Rademaker C Successful cord blood transplantation in a premature and dysmature neonate of 1700 g with reticulardysgenesis. Bone Marrow Transplant. 2007;39:307–308.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.