Diseases and Disorders, Porphyrias and Bilirubinemias
Last Updated: October 30, 2025 Introduction to Porphyria Cutanea Tarda Porphyria cutanea tarda (PCT) is an autosomal dominant disorder that is a member of a family of disorders referred to as the porphyrias. Each disease in this family results from deficiencies in a...
Diseases and Disorders, Porphyrias and Bilirubinemias
Last Updated: October 30, 2025 Introduction to Congenital Erythropoietic Porphyria Congenital erythropoietic porphyria, CEP (also referred to as Günther disease) is inherited as an autosomal recessive disorder. CEP a disorder that is a member of a family of disorders...
Diseases and Disorders, Porphyrias and Bilirubinemias
Last Updated: October 30, 2025 Introduction to Acute Intermittent Porphyria Acute intermittent porphyria (AIP) is a disorder that is a member of a family of disorders referred to as the porphyrias. Each disease in this family results from deficiencies in a specific...
Diseases and Disorders, Porphyrias and Bilirubinemias
Last Updated: October 30, 2025 Introduction to ALA Dehydratase Deficient Porphyria, ADP ALA dehydratase deficient porphyria (ADP) is an autosomal recessive disorder that is a member of a family of disorders referred to as the porphyrias. Each disease in this family...
Diseases and Disorders, Porphyrias and Bilirubinemias
Last Updated: October 30, 2025 Introduction to X-Linked Sideroblastic Anemia, XLSA X-linked sideroblastic anemia (XLSA) is a recessive disorder that results from deficiencies in the erythroid-specific form of δ-aminolevulinic acid synthase (also called...
