Related Experiment Video
Updated: Jan 11, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Unlocking Rare Diagnoses: The Essential Role of Molecular Techniques in Hemoglobin Agrinio. A Case Report
Marta Moreno Carbonell1, Ana Gómez Martínez2, Sergio Felipe Pinzón Mariño3
1Haematology Department, Hospital Universitario Insular de Gran Canaria, Las Palmas de Gran Canaria, Spain.
Abstract:
Alpha thalassemia is characterized by the reduced or absent synthesis of alpha globin chains, most commonly due to deletional mutations. Hb Agrinio [α29(B10) Leu→Pro, CTG>CCG (α2)] is an infrequent nondeletional alpha thalassemia (α-Thal) that has been described in less than 20 individuals in the world. We presented the case of a girl with anemia since birth and high transfusion needs, with a recent diagnosis of homozygous Hb Agrinio.
More Related Videos
11:59Detection of Residual Donor Erythroid Progenitor Cells after Hematopoietic Stem Cell Transplantation for Patients with Hemoglobinopathies
Published on: September 6, 2017
05:18A Rapid and Chemical-free Hemoglobin Assay with Photothermal Angular Light Scattering
Published on: December 7, 2016
Related Concept Videos
Blood Transfusion and Agglutination
History
The history of blood transfusion dates back to the 17th century, when early attempts were made in animals. In 1818 James Blundell, a British doctor, performed the first successful human blood transfusion. Later in 1900, Karl...
Blood Typing
Antigens are protein molecules that reside on the surface of red blood cells (RBCs). The ABO and Rh blood typing systems target...
Karyotyping
Methods of Classification and Identification
Gene Families
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...