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Hb H Disease Diagnosed During Adolescent Pregnancy.

Tekin AksuÇağrı CoşkunBulent Baris KuskonmazSule UnalŞevkiye Selin AytaçFatma Gumruk
Published in: Hemoglobin (2020)
Hb H disease is a moderate to severe form of α-thalassemia (α-thal). Patients with Hb H disease may become symptomatic, especially during infections and pregnancy, and may require transfusions. Herein, we present a 16-year-old female with Hb H disease who was initially diagnosed during adolescent pregnancy and was found to carry the -α3.7/-(α)20.5 deletions. The relatively mild presentation of this case highlights the milder phenotypic consequences of deletional α mutations. The case describes the screening and management of pregnancy with Hb H disease. Additionally, this case demonstrates that screening of some undiagnosed inherited blood disorders is important during pregnancy.
Keyphrases
  • preterm birth
  • young adults
  • mental health
  • pregnancy outcomes
  • high intensity
  • sickle cell disease