Clinical and molecular characteristics of imerslund‐gräsbeck syndrome: First report of a novel Frameshift variant in Exon 11 of AMN gene

Clinical and molecular characteristics of imerslund‐gräsbeck syndrome: First report of a novel Frameshift variant in Exon 11 of AMN gene

Introduction Imerslund‐Gräsbeck syndrome (IGS) is a rare autosomal‐recessive disorder characterized by selective vitamin B12 malabsorption, megaloblastic anemia, and proteinuria. The precise incidence of this disorder is unknown in the Middle East and Arab countries. The disease is caused by a homoz...

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Bibliographic Details
Published in:International journal of laboratory hematology Vol. 43; no. 5; pp. 1009 - 1015
Main Authors: Elshinawy, Mohamed, Gao, Harry H., Al‐Nabhani, Dana M., Al‐Thihli, Khalid A.
Format: Journal Article
Language:English
Published: England Wiley Subscription Services, Inc 01-10-2021
Subjects:
AMN gene
Anemia
Consanguinity
Folic acid
Frameshift mutation
Genes
Genetic variability
Hereditary diseases
Heterozygotes
Imerslund‐Gräsbeck syndrome
Malabsorption
megaloblastic anemia
Patients
Proteinuria
Vitamin B12
Vitamin deficiency
Imerslund-Gräsbeck syndrome
AMN gene
megaloblastic anemia
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Summary:Introduction Imerslund‐Gräsbeck syndrome (IGS) is a rare autosomal‐recessive disorder characterized by selective vitamin B12 malabsorption, megaloblastic anemia, and proteinuria. The precise incidence of this disorder is unknown in the Middle East and Arab countries. The disease is caused by a homozygous variant in either AMN or CUBN genes. In addition, some compound heterozygous variants are reported. Methods Clinical and laboratory data of patients diagnosed with IGS in Oman were retrospectively collected. Mutation analysis for all genes involved in vitamin B12/folic acid metabolism and megaloblastic anemia was conducted using next‐generation sequencing (NGS). Results Three siblings (2 girls and a boy) have been diagnosed with the condition. They exhibit a phenotypic variability with different age of presentation and different spectrum of disease. All patients harbor a novel biallelic frameshift mutation in exon 11 of AMN gene (p.Pro409Glyfs*), which was not reported previously in the literature. Both parents are heterozygotes for the same variant. All patients responded well to vitamin B12 parenteral therapy, but proteinuria persisted. Conclusion In communities with high incidence of consanguinity, cases of early‐onset vitamin B12 deficiency should be thoroughly investigated to explore the possibility of Imerslund‐Gräsbeck syndrome and other vitamin B12–related hereditary disorders. Further local and regional studies are highly recommended.
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ISSN:1751-5521
1751-553X
DOI:10.1111/ijlh.13473