Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome

Pulmonary fibrosis - hepatic hyperplasia - bone marrow hypoplasia, also named Btrimorphic syndromeB (i.e. three (inherited) morbidities, pulmonary, hepatic and cytopenia), is a rare disease reported in 4 cases to date, manifesting with idiopathic pulmonary fibrosis, hepatic nodular regenerative hyperplasia leading to portal hypertension and thrombocytopenia due to bone marrow hypoplasia. The condition was associated with 100% mortality.

60 clinical trials for this condition and its sub-types, 0 tagged with Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome itself.