| Literature DB >> 28405076 |
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