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.
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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.
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Bei dem Ceelen-Gellerstedt-Syn ...... rimäre Hämosiderose der Lunge.
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Idiopathic pulmonary haemoside ...... 1.23 cases per million people.
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La hemosiderosis pulmonar idio ...... ia en los casos más avanzados.
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Pierwotna samoistna hemosydero ...... adzona w 1944 przez Selandera.
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特発性肺ヘモジデローシス（とくはつせいはいへもじでろーしす、 ...... に稀で、我が国においては「123万人に1人」との調査がある。
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723,401,045
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Bei dem Ceelen-Gellerstedt-Syn ...... rimäre Hämosiderose der Lunge.
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Idiopathic pulmonary haemoside ...... 1.23 cases per million people.
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La hemosiderosis pulmonar idio ...... piratoria en los casos más ava
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Pierwotna samoistna hemosydero ...... polega na podawaniu sterydów.
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特発性肺ヘモジデローシス（とくはつせいはいへもじでろーしす、 ...... に稀で、我が国においては「123万人に1人」との調査がある。
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Ceelen-Gellerstedt-Syndrom
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Hemosiderosis pulmonar idiopática
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Idiopathic pulmonary haemosiderosis
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Pierwotna samoistna hemosyderoza płucna
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特発性肺ヘモジデローシス
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Idiopathic pulmonary hemosiderosis
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