A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant

Eitemau Tebyg

• Interesting case of G6PD deficiency anemia with severe hemolysis
  gan: Chhabra, Anupam, et al.
  Cyhoeddwyd: (2013)
• No evidence that chloroquine or hydroxychloroquine induce hemolysis in G6PD deficiency()
  gan: Schilling, William H.K., et al.
  Cyhoeddwyd: (2020)
• “Hemolysis, or not Hemolysis, that is the Question”. Use of Hydroxychloroquine in a Patient with COVID-19 Infection and G6PD Deficiency
  gan: Sgherza, Nicola, et al.
  Cyhoeddwyd: (2020)
• Val-Gly-Val-Ala-Pro-Gly, a repeating peptide in elastin, is chemotactic for fibroblasts and monocytes
  Cyhoeddwyd: (1984)
• Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family
  gan: Dongerdiye, Rashmi, et al.
  Cyhoeddwyd: (2021)