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Erythropoietic protoporphyria

Erythropoietic protoporphyria (EPP) was first described in 1953, when kosenew and others called it "atypical summer blister disease". In 1961, Magnus et al. Identified it as an independent porphyria and named it EPP.

Symptoms

Suppurative osteomyelitis

Necrotizing sarcoidosis like granulomatosis

Mixed porphyria

Acquired circulating anticoagulant syndrome

Cavernous hemangioma thrombocytopenia syndrome

Acquired vitamin K-dependent coagulation factor abnormality

Acquired circulating anticoagulant syndrome

Acquired platelet dysfunction

acquired hemophilia

Pyrimidine 5 '- nucleotide deficiency

Huntington's disease dementia

IgA nephropathy

Type II renal tubular acidosis

Type I renal tubular acidosis

Type I diabetes mellitus

Myoclonus

cervical spondylopathy

hyperthyroidism

Alcoholic liver

thyroiditis

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