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. 2020 Mar 14:hcaa094. doi: 10.1093/qjmed/hcaa094
Osler-Weber-Rendu Syndrome
Babu Ivan Mani
1,✉, Abdur Rahman Rubel
1, Waqas Ahmed Chauhdary
1, Aieman Bashir
1, Zar Ni Soe
1, Nasir Javed
1, Shah Muhammad Alam Sharif
1, May Thu Hla Aye
1, Vui Heng Chong
1
Babu Ivan Mani
1Department of Medicine, PMMPHAMB Hospital, Jalan Sungai Basong, Tutong, Brunei Darussalam
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Abdur Rahman Rubel
1Department of Medicine, PMMPHAMB Hospital, Jalan Sungai Basong, Tutong, Brunei Darussalam
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Waqas Ahmed Chauhdary
1Department of Medicine, PMMPHAMB Hospital, Jalan Sungai Basong, Tutong, Brunei Darussalam
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Aieman Bashir
1Department of Medicine, PMMPHAMB Hospital, Jalan Sungai Basong, Tutong, Brunei Darussalam
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Zar Ni Soe
1Department of Medicine, PMMPHAMB Hospital, Jalan Sungai Basong, Tutong, Brunei Darussalam
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Nasir Javed
1Department of Medicine, PMMPHAMB Hospital, Jalan Sungai Basong, Tutong, Brunei Darussalam
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Shah Muhammad Alam Sharif
1Department of Medicine, PMMPHAMB Hospital, Jalan Sungai Basong, Tutong, Brunei Darussalam
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May Thu Hla Aye
1Department of Medicine, PMMPHAMB Hospital, Jalan Sungai Basong, Tutong, Brunei Darussalam
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Vui Heng Chong
1Department of Medicine, PMMPHAMB Hospital, Jalan Sungai Basong, Tutong, Brunei Darussalam
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1Department of Medicine, PMMPHAMB Hospital, Jalan Sungai Basong, Tutong, Brunei Darussalam
✉
Correspondence author: Babu Ivan MANI, E-mail: babuivan@gmail.com
Received 2020 Mar 4; Accepted 2020 Mar 8.
Keywords: Epistaxis, Chronic iron deficiency anaemia, Telangiectasia, Arterio-venous malformations, Hereditary Haemorrhagic Telangiectasia
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PMCID: PMC7094783 PMID: 32170936