A case report of hereditary spherocytosis affecting mother and child with varied severity

  • Dr Venkatamurthy M Adichunchanagiri Institute of Medical Sciences, B.G. Nagara, Nagamangala Taluk, Mandya District, Karnataka, India.
  • Dr B Aditya Kumar Adichunchanagiri Institute of Medical Sciences, B.G. Nagara, Nagamangala Taluk, Mandya District, Karnataka, India.
Keywords: Hereditary spherocytosis (HS), Hemolytic anemia, Autosomal Dominant

Abstract

Hereditary spherocytosis (HS) is a genetically transmitted form of spherocytosis, an autohemolytic anemia characterized by the production of red blood cells that are sphere-shaped rather than biconcave disc, and therefore more prone to hemolysis. It is a result of heterogeneous alterations in one of six genes (most often the ankyrin gene) that encode for proteins involved in vertical associations that tie the membrane skeleton to the lipid bilayer. We report a case of Heriditary spherocytosis affecting both mother and the baby with varied severity.

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References

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A case report of hereditary spherocytosis affecting mother and child with varied severity
CITATION
DOI: 10.17511/ijpr.2017.i07.10
Published: 2017-07-31
How to Cite
Dr Venkatamurthy M, & Dr B Aditya Kumar. (2017). A case report of hereditary spherocytosis affecting mother and child with varied severity. Pediatric Review: International Journal of Pediatric Research, 4(7), 494-496. https://doi.org/10.17511/ijpr.2017.i07.10
Section
Case Report