Paroxysmal nocturnal haemoglobinuria associated with a novel phosphatidylinositol glycan class A (PIGA) mutation in a patient with Klinefelter syndrome

Ann Hematol. 2021 Jun;100(6):1625-1627. doi: 10.1007/s00277-020-04377-9. Epub 2021 Jan 8.

Authors

Yotaro Tamai¹, Sayaka Ito^{2

3}, Atsuhiko Hasegawa³

Affiliations

¹ Department of Hematology, Shonan Kamakura General Hospital, 1370-1 Okamoto, Kamakura, Kanagawa, 247-8533, Japan. y_tamai@shonankamakura.or.jp.
² Department of Medical Technology, Tokyo University of Technology School of Health Sciences, Tokyo, Japan.
³ Department of Immunotherapeutics, Tokyo Medical and Dental University, Tokyo, Japan.

PMID: 33416903
DOI: 10.1007/s00277-020-04377-9

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adult
Hemoglobinuria, Paroxysmal / complications
Hemoglobinuria, Paroxysmal / genetics*
Humans
Klinefelter Syndrome / complications
Klinefelter Syndrome / genetics*
Male
Membrane Proteins / genetics*
Mutation

Substances

Membrane Proteins
phosphatidylinositol glycan-class A protein