Hereditary Hemorrhagic Telangiectasia as a Rare Cause of Iron Deficiency Anemia: a Case Report

Volume: 1 Number: 1 January 1, 2017
  • Muammer Bilici
  • Murat Güllü
  • İbrahim İlker Öz
  • Sevil Uygun İlikhan
  • Ali Borazan
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Medical Journal of Western Black Sea
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Hereditary Hemorrhagic Telangiectasia as a Rare Cause of Iron Deficiency Anemia: a Case Report

Abstract

Hereditary hemorrhagic telangiectasia (HHT), also known as OslerWeber-Rendu syndrome is an autosomal-dominant multi-organ vascular dysplasia and results in a tendency for bleeding. The worldwide prevalence is 1-2 cases per 100 000 population. However most patients have a normal life expectancy. HHT can lead to serious or even life-threatening complications such as stroke, cerebral abscess or massive haemorrhage in almost 10% of patients. Here, we reported a patient presented with HHT causing iron deficiency anemia

Details

Primary Language

English

Subjects

-

Journal Section

-

Authors

Muammer Bilici This is me

Murat Güllü This is me

İbrahim İlker Öz This is me

Sevil Uygun İlikhan This is me

Ali Borazan This is me

Publication Date

January 1, 2017

Submission Date

January 1, 2017

Acceptance Date

-

Published in Issue

Year 2017 Volume: 1 Number: 1

IZ

https://izlik.org/JA46HG93YK

Cite

RIS / Bibtex
APA
Bilici, M., Güllü, M., Öz, İ. İ., İlikhan, S. U., & Borazan, A. (2017). Hereditary Hemorrhagic Telangiectasia as a Rare Cause of Iron Deficiency Anemia: a Case Report. Medical Journal of Western Black Sea, 1(1), 1-5. https://izlik.org/JA46HG93YK
AMA
1.Bilici M, Güllü M, Öz İİ, İlikhan SU, Borazan A. Hereditary Hemorrhagic Telangiectasia as a Rare Cause of Iron Deficiency Anemia: a Case Report. Med J West Black Sea. 2017;1(1):1-5. https://izlik.org/JA46HG93YK
Chicago
Bilici, Muammer, Murat Güllü, İbrahim İlker Öz, Sevil Uygun İlikhan, and Ali Borazan. 2017. “Anemia: A Case Report”. Medical Journal of Western Black Sea 1 (1): 1-5. https://izlik.org/JA46HG93YK.
EndNote
Bilici M, Güllü M, Öz İİ, İlikhan SU, Borazan A (January 1, 2017) Hereditary Hemorrhagic Telangiectasia as a Rare Cause of Iron Deficiency Anemia: a Case Report. Medical Journal of Western Black Sea 1 1 1–5.
IEEE
[1]M. Bilici, M. Güllü, İ. İ. Öz, S. U. İlikhan, and A. Borazan, “Hereditary Hemorrhagic Telangiectasia as a Rare Cause of Iron Deficiency Anemia: a Case Report”, Med J West Black Sea, vol. 1, no. 1, pp. 1–5, Jan. 2017, [Online]. Available: https://izlik.org/JA46HG93YK
ISNAD
Bilici, Muammer - Güllü, Murat - Öz, İbrahim İlker - İlikhan, Sevil Uygun - Borazan, Ali. “Anemia: A Case Report”. Medical Journal of Western Black Sea 1/1 (January 1, 2017): 1-5. https://izlik.org/JA46HG93YK.
JAMA
1.Bilici M, Güllü M, Öz İİ, İlikhan SU, Borazan A. Hereditary Hemorrhagic Telangiectasia as a Rare Cause of Iron Deficiency Anemia: a Case Report. Med J West Black Sea. 2017;1:1–5.
MLA
Bilici, Muammer, et al. “Anemia: A Case Report”. Medical Journal of Western Black Sea, vol. 1, no. 1, Jan. 2017, pp. 1-5, https://izlik.org/JA46HG93YK.
Vancouver
1.Muammer Bilici, Murat Güllü, İbrahim İlker Öz, Sevil Uygun İlikhan, Ali Borazan. Hereditary Hemorrhagic Telangiectasia as a Rare Cause of Iron Deficiency Anemia: a Case Report. Med J West Black Sea [Internet]. 2017 Jan. 1;1(1):1-5. Available from: https://izlik.org/JA46HG93YK

The Western Black Sea Medical Journal is an international, peer-reviewed, and open-access journal published by Zonguldak Bülent Ecevit University. First launched in 2017, the journal is published three times a year (in April, August, and December) and accepts articles in both Turkish and English.