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Recurrent Paradoxical Embolism and Manganese Deposition in the Basal Ganglia in a Patient with Hereditary Haemorrhagic Telangiectasias: A Case Report and Literature Review

2023-10-11

Abstract excerpt

<title>Abstract</title> <p>Background Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant inherited vascular disorder that can involve multiple organs, thus can be associated with so many clinical departments that proper screening and diagnosis of HHT are needed for providing better management of both patients and their family members. Case presentation: we present a 58-year-old female pati...

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Literature Corpus work
4c782382-d76b-5948-9221-86ea70a3884e
DOI
10.21203/rs.3.rs-3409570/v1
Open publication

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Recurrent Paradoxical Embolism and Manganese Deposition in the Basal Ganglia in a Patient with Hereditary Haemorrhagic Telangiectasias: A Case Report and Literature ReviewDOI 10.21203/rs.3.rs-3409570/v1
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