Idiopathic pulmonary haemosiderosis
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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