1 results match your criteria: "Adult Inherited Metabolic Diseases Salford Royal Hospital NHS Trust Salford UK.[Affiliation]"
Acaeruloplasminemia is a rare autosomal recessive condition caused by inactivating mutations of the gene encoding caeruloplasmin (ferroxidase). Caeruloplasmin is a copper-containing plasma ferroxidase enzyme with a key role in facilitating cellular iron efflux. We describe a case of a patient with acaeruloplasminemia, confirmed by genetic analysis, treated with combination therapy of monthly fresh-frozen plasma (FFP) or Octaplas and iron chelation over a 3-year period.
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