Publicidad

Hallazgos de la gammagrafia ósea con 99mTc-HDP en un paciente pediátrico con síndrome falciforme (Hb S/ Beta talasemia)

Referencias

  1. Modell B, Darlison M, Birgens H, et al. Epidemiology of haemoglobin disorders in Europe: an overview. Scand J Clin Lab Invest. 2007;67:39-69.
  2. Mikosch P, Jauk B, Kaulfersch W, et al. Scintigraphic findings in a patient with sickle-cell thalassemia and reccurent pain attacks. Wien Med Wochenschr 2003; 3-4:83-8.
  3. Ahmed H. Al-Salem. Splenic complications of sickle cell anemia and the role of splenectomy. ISRN Hematol. 2011; 2011: 864257.