Aceruloplasminemia | Familial Apoceruloplasmin | Hereditary Ceruloplasmin
Aceruloplasminemia is generally described as a rare genetic disorder in which there is an unusual accumulation of large amounts of iron in the brain and other inner organs. Mainly, this disorder affects neurological symptoms like cognitive impairment and movement disorders and some retina degradation and also it causes diabetes. Aceruloplasminemia is also called familial apoceruloplasmin otherwise it is called hereditary ceruloplasmin deficiency. Typically, Aceruloplasminemia is a rare type of genetic disorder that is inherited by the people who have Aceruloplasminemia disease will receive by autosomal recessive pattern which means it is received by one or both biological parents who are carriers of the mutated genes. The main cause of the illness is unusual or abnormal change in the ceruloplasmin (CP) gene pattern. Autosomal recessive disease is a pattern of inheritance where the person who is affected can possess two copies of the mutated gene. But this disorder can pass down o...