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Multiple endocrine neoplasia type 1 syndrome due to novel Alu insertion
Aislinn Cragg1, Hannah Boon2, Treena Cranston2
1Faculty of Medicine, University of Southampton, Southampton, Hampshire, UK.
Abstract:
Multiple Endocrine Neoplasia type 1 syndrome is caused by pathogenic variants in the MEN1 gene, and is characterised by tumours in multiple endocrine glands. This case study looks at a family with four affected members over two generations who have been diagnosed with the syndrome after next generation sequencing identified a novel Alu insertion. Previous genetic testing in the index patient had not identified an underlying cause.
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