Idiopathic pulmonary haemosiderosis

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Idiopathic pulmonary haemosiderosis (or idiopathic pulmonary hemosiderosis; IPH) is a lung disease of unknown cause that is characterized by alveolar capillary bleeding and accumulation of haemosiderin in the lungs. It is rare with an incidence between 0.24 and 1.23 cases per million people.
Links
https://en.wikipedia.org/wiki/Idiopathic pulmonary haemosiderosis
Relevant Occupations
Respiratory and Sleep Medicine Specialist
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