Type I congenital methemoglobinemia in a Chinese family

Ann Hematol. 2021 Sep;100(9):2417-2419. doi: 10.1007/s00277-020-04141-z. Epub 2020 Jun 17.

Authors

Jiang Ji¹, Yang Liu², Miao Chen³

Affiliations

¹ Department of Hematology, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing, China.
² Department of Hematology, Peking University People's Hospital, Beijing, China.
³ Department of Hematology, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing, China. [email protected].

PMID: 32556454
DOI: 10.1007/s00277-020-04141-z

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Asian People / genetics
China
Cyanosis / diagnosis
Cyanosis / genetics
Cytochrome-B(5) Reductase / genetics
Female
Humans
Male
Methemoglobinemia / congenital*
Methemoglobinemia / diagnosis
Methemoglobinemia / genetics
Middle Aged
Mutation
Pedigree

Substances

CYB5R3 protein, human
Cytochrome-B(5) Reductase

Supplementary concepts

Congenital Methemoglobinemia

Grants and funding

81970106/National Natural Science Foundation of China