Hb G-Waimanalo [A1] or α64(E13)Asp→Asn (α1) (HBA1: c.193G>A) Observed in a Bulgarian Family

Hemoglobin. 2015;39(6):430-1. doi: 10.3109/03630269.2015.1066685. Epub 2015 Jul 27.

Abstract

The abnormal hemoglobin (Hb) with an aspartic acid to asparagine substitution at α64 has been found on both the α2- and α1-globin genes. It has been described in many different populations under different names, but never in Bulgaria. Using the recently proposed nomenclature, Hb G-Waimanalo [A1] refers to the HBA1: c.193G > A, while Hb G-Waimanalo [A2] refers to the HBA2: c.193G > A mutation. Here, we present the first family from Bulgaria with Hb G-Waimanalo [A1].

Keywords: Hb Burgos; Hb G-Waimanalo; Hb Wädenswil; hemoglobin (Hb) variant.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Anemia, Hypochromic / diagnosis
  • Anemia, Hypochromic / genetics
  • Bulgaria
  • Child
  • Child, Preschool
  • DNA Mutational Analysis
  • Erythrocyte Indices
  • Family
  • Female
  • Genotype
  • Glycated Hemoglobin / genetics*
  • Hemoglobins, Abnormal / genetics*
  • Humans
  • Male
  • Mutation*
  • Phenotype
  • Young Adult
  • alpha-Globins / genetics*

Substances

  • Glycated Hemoglobin A
  • Hemoglobins, Abnormal
  • alpha-Globins
  • hemoglobin G Waimanalo