Severe congenital neutropenia with mastoidectomy: A case report of HAX1

Klin Padiatr. 2021 Nov;233(6):303-305. doi: 10.1055/a-1479-2692. Epub 2021 Jun 8.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Congenital Bone Marrow Failure Syndromes
  • Humans
  • Mastoidectomy*
  • Mutation
  • Neutropenia* / congenital

Substances

  • Adaptor Proteins, Signal Transducing
  • HAX1 protein, human

Supplementary concepts

  • Neutropenia, Severe Congenital, Autosomal Recessive 3