The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
Orpha Number: 251375
A rare, genetic hemoglobinopathy usually characterized by mild hemolysis without vaso-occlusive complications or abnormality of red blood cell morphology. However, more severe manifestations have also been reported, including hematuria, splenic infarction, acute chest syndrome, acute episodes of pain and reversible bone marrow necrosis.
Visit the Orphanet disease page for more resources.
Source: GARD Last updated on 05-01-20
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