Literature DB >> 28405076

A rare hemoglobin variant, Hb Belliard.

Stacey Murthy1, Raul Benavides1.   

Abstract

There are many documented variants of hemoglobin; however, other than a limited number (such as sickle cell disease), very few are known to have any clinical significance. As advances in detection and identification continue through gel electrophoresis, capillary electrophoresis, and DNA sequencing, more rare variants are identified. Without case reporting, the significance of these variants will remain unknown or continue to be thought of as insignificant. Here we report a rare hemoglobin variant, Hb Belliard, which was detected in a 68-year-old Indian immigrant to the United States. He presented with elevated hemoglobin and was found to have a unique peak on capillary electrophoresis. The specimen was sent for sequencing and was subsequently found to have Hb Belliard. Currently, Hb Belliard is thought to be insignificant.

Year:  2017        PMID: 28405076      PMCID: PMC5349822          DOI: 10.1080/08998280.2017.11929577

Source DB:  PubMed          Journal:  Proc (Bayl Univ Med Cent)        ISSN: 0899-8280


  2 in total

1.  Hb Belliard [alpha 56(E5)Lys----Asn] a new fast-moving alpha chain variant found in a subject of Spanish origin.

Authors:  H Wajcman; G Gombaud-Saintonge; F Galacteros; M Martha; F Vertongen
Journal:  Hemoglobin       Date:  1989       Impact factor: 0.849

Review 2.  Abnormal haemoglobins: detection & characterization.

Authors:  Henri Wajcman; Kamran Moradkhani
Journal:  Indian J Med Res       Date:  2011-10       Impact factor: 2.375

  2 in total

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