Characterization and identification of Hb Bart's hydrops fetalis caused by a compound heterozygous mutation --SEA /--CR , a novel α0 -thalassemia deletion.

• Authors: Chedtapak Ruengdit, Sitthichai Panyasai, Naowarat Kunyanone, Worawich Phornsiricharoenphant, Chumpol Ngamphiw, Sissades Tongsima, Orapan Sripichai, Serge Pissard, Sakorn Pornprasert
• Journal: International journal of laboratory hematology (Int J Lab Hematol) Vol. 42 Issue 3 Pg. e116-e120 (06 2020) ISSN: 1751-553X [Electronic] England
• PMID: 31943793 (Publication Type: Letter, Research Support, Non-U.S. Gov't)

Chemical References

• Hemoglobins, Abnormal
• hemoglobin Bart's

Topics

• Female
• Hemoglobins, Abnormal (genetics)
• Heterozygote
• Humans
• Hydrops Fetalis (diagnosis, genetics)
• Mutation
• Pregnancy
• Prenatal Diagnosis
• alpha-Thalassemia (diagnosis, genetics)