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Hereditary Coproporphyria (Coproporphyrinogen Oxidase Deficiency)

An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features include both neurological symptoms and cutaneous lesions. Patients excrete increased levels of porphyrin precursors, 5-AMINOLEVULINATE and COPROPORPHYRINS.
Also Known As:
Coproporphyrinogen Oxidase Deficiency; Coproporphyria, Hereditary; Deficiency, Coproporphyrinogen Oxidase
Networked: 149 relevant articles (5 outcomes, 8 trials/studies)

Relationship Network

Disease Context: Research Results

Related Diseases

1. Acute Intermittent Porphyria (Porphyria, Acute)
2. Erythropoietic Porphyria (Congenital Erythropoietic Porphyria)
3. Variegate Porphyria (Protoporphyrinogen Oxidase Deficiency)
4. Porphyria Cutanea Tarda
5. Erythropoietic Protoporphyria

Experts

1. Bonkovsky, Herbert L: 5 articles (11/2019 - 01/2005)
2. Puy, Hervé: 5 articles (11/2019 - 01/2002)
3. Doss, M O: 5 articles (12/2010 - 08/2000)
4. Desnick, Robert J: 4 articles (11/2019 - 02/2011)
5. Deybach, Jean-Charles: 4 articles (11/2019 - 01/2002)
6. Gross, U: 4 articles (01/2003 - 08/2000)
7. Anderson, Karl E: 3 articles (01/2022 - 01/2006)
8. Stölzel, Ulrich: 3 articles (11/2021 - 01/2019)
9. Chen, Brenden: 3 articles (11/2019 - 11/2019)
10. Gouya, Laurent: 3 articles (11/2019 - 02/2004)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Hereditary Coproporphyria:
1. PorphyrinsIBA
2. Acute Hepatic PorphyriaIBA
3. AcidsIBA
4. Ligases (Synthetase)IBA
5. Hormones (Hormone)IBA
6. Erythromycin (Erycette)FDA LinkGeneric
7. Hormonal Oral ContraceptivesIBA
8. Coproporphyrinogen Oxidase (Coproporphyrinogen III Oxidases)IBA
9. Oxidoreductases (Dehydrogenase)IBA
10. PorphobilinogenIBA

Therapies and Procedures

1. Therapeutics
2. Kidney Transplantation
3. Radiotherapy
4. Renal Dialysis (Hemodialysis)
5. Appendectomy