Search results for: Yoshinao Wada
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Hereditary ceruloplasmin deficiency with hemosiderosis
Human Genetics > 1996 > 97 > 6 > 755-758
Abstract Hereditary ceruloplasmin deficiency with hemosiderosis (aceruloplasminemia) is a new disease characterized by systemic hemosiderosis, diabetes mellitus, neurological abnormalities and pigment degeneration of the retina. Loss of the ferroxidase activity of ceruloplasmin results in systemic iron deposition and tissue damage. Neuroimaging studies reveal iron deposition in basal ganglia and in...
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