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Pulmonary Haemosiderosis Secondary to Hereditary Haemochromatosis; a Case Report Cover

Pulmonary Haemosiderosis Secondary to Hereditary Haemochromatosis; a Case Report

Journal of Cancer and Allied Specialties
Volume 6 (2020): Issue 1 (January 2020)
By: Waqas Jehangir,  Alexander D. Karabachev and  Elvira R. Umyarova  
Open Access
|Jan 2020

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DOI: https://doi.org/10.37029/jcas.v6i1.281 | Journal eISSN: 2411-989X
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Language: English
Page range: 1 - 5
Submitted on: Sep 1, 2019
Accepted on: Nov 29, 2019
Published on: Jan 5, 2020
Published by: Shakuat Khanum Memorial Cancer Hospital and Research Centre
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Dyspnoea,
ferritins,
haemochromatosis protein,
haemochromatosis,
haemosiderosis,
mutation
Related subjects:
Medicine,
Clinical medicine,
Internal medicine,
Internal medicine, other,
Haematology, oncology,
Pediatrics and juvenile medicine,
Paediatric haematology and oncology,
Surgery,
Surgery, other

© 2020 Waqas Jehangir, Alexander D. Karabachev, Elvira R. Umyarova, published by Shakuat Khanum Memorial Cancer Hospital and Research Centre
This work is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License.

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