A novel mutation of glucose phosphate isomerase (GPI) causing severe neonatal anemia due to GPI deficiency

Nienke C. M. Burger, Richard van Wijk, Dorine Bresters, Eveline A. Schell

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Glucose-6-phosphate isomerase (GPI) deficiency is very rare, but one of the most common erythroenzymopathies, causing hereditary nonspherocytic hemolytic anemia. This case report describes the clinical features and the molecular etiology of a Dutch patient with GPI deficiency. She is the fifth patient with GPI deficiency identified to date in the Netherlands and was found to be compound heterozygous for the previously reported c.1615G>A p. (Asp539Asn) mutation and a novel c.271A>T p.(Asn91Tyr) variant.
Original languageEnglish
Pages (from-to)E186-E189
JournalJournal of Pediatric Hematology / Oncology
Volume41
Issue number3
DOIs
Publication statusPublished - 1 Apr 2019
Externally publishedYes

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