Pulmonary Haemosiderosis Secondary to Hereditary Haemochromatosis; a Case Report

INTRODUCTION: Hereditary haemochromatosis (HH) is an autosomal recessive disease of increased intestinal absorption of iron, leading to accumulation in tissues which may progress to organ damage, most commonly in the liver. Iron deposition in the liver can lead to cirrhosis and hepatocellular carcin...

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Detalles Bibliográficos
Autores principales: Jehangir, Waqas, Karabachev, Alexander D., Umyarova, Elvira R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore. Pakistan 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166317/
https://www.ncbi.nlm.nih.gov/pubmed/37197141
http://dx.doi.org/10.37029/jcas.v6i1.281

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166317/
https://www.ncbi.nlm.nih.gov/pubmed/37197141
http://dx.doi.org/10.37029/jcas.v6i1.281

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