A rare diagnosis: Hermansky-Pudlak syndrome in a patient with pulmonary fibrosis, oculocutaneous albinism and thrombocytopathy
M. Doubková (Brno, Czech Republic), J. Trizuljak (Brno, Czech Republic), A. Hrazdirová (Brno, Czech Republic), Z. Vrzalová (Brno, Czech Republic), I. Blaháková (Brno, Czech Republic), L. Radová (Brno, Czech Republic), Š. Pospíšilová (Brno, Czech Republic), M. Doubek (Brno, Czech Republic)
Source: International Congress 2019 – The changing face of rare diffuse parenchymal lung diseases: recent advances in pathogenesis, clinical manifestations and treatment
Disease area: Interstitial lung diseases, Paediatric lung diseases
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M. Doubková (Brno, Czech Republic), J. Trizuljak (Brno, Czech Republic), A. Hrazdirová (Brno, Czech Republic), Z. Vrzalová (Brno, Czech Republic), I. Blaháková (Brno, Czech Republic), L. Radová (Brno, Czech Republic), Š. Pospíšilová (Brno, Czech Republic), M. Doubek (Brno, Czech Republic). A rare diagnosis: Hermansky-Pudlak syndrome in a patient with pulmonary fibrosis, oculocutaneous albinism and thrombocytopathy. 1400
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