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Autoimmune hemolytic anemia and thrombocytopenia in a Chinese patient with heterozygous NBAS mutations: Case report.

Yuanlin YangXiaoming FeiFang LeiLixia WangXianqiu YuYu Tang
Published in: Medicine (2024)
The phenotype of this case indicates that c.335 + 1G>A NBAS variant is probably a pathogenic one and c.2356C>T ANKRD26 variant is improbably a pathogenic one. AIHA may respond well to steroid even when happened in patients with NBAS disease.
Keyphrases
  • case report
  • chronic kidney disease
  • early onset
  • multiple sclerosis
  • iron deficiency
  • drug induced