• Media type: E-Article
  • Title: Hemoglobinopathy SD presenting as Hemoglobinopathy SS
  • Contributor: Lissa, Sonia Maria; Bach, Sergio Luiz; Spezia, Juliana; Henneberg, Railson; Silva, Paulo Henrique da
  • imprint: Universidade de Sao Paulo, Agencia USP de Gestao da Informacao Academica (AGUIA), 2017
  • Published in: Medicina (Ribeirão Preto)
  • Language: Not determined
  • DOI: 10.11606/issn.2176-7262.v50i3p177-181
  • ISSN: 2176-7262; 0076-6046
  • Keywords: General Medicine
  • Origination:
  • Footnote:
  • Description: <jats:p>This case report shows the interaction of hemoglobin (Hb) S with Hb D. in a child previously diagnosed with sickle cell anemia based on the Hb electrophoretic migration pattern in alkaline pH. The sickling phenomenon was confirmed with 2% sodium metabisulfite. The father and mother of the child had a heterozygous pattern (Hb AS) in hemoglobin electrophoresis at alkaline pH. The sickling phenomenon has been confirmed to the father, but it has not been confirmed for the mother. The electrophoresis at acid pH was used to differentiate Hb S from Hb D. The family’s phenotype was established: the father has Hb AS, the mother AD and, the child SD. The purpose of this study was to emphasize the importance of confirmation of Hb S detected in electrophoresis at alkaline pH, with the solubility test or 2% sodium metabisulfite and with the electrophoresis at acid pH.</jats:p>
  • Access State: Open Access