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Congenital erythropoietic porphyria in Adult
Other Resources UpToDate PubMed

Congenital erythropoietic porphyria in Adult

Contributors: Joe Tung, Susan Burgin MD
Other Resources UpToDate PubMed

Synopsis

Gunther disease, also called congenital erythropoietic porphyria, is a rare autosomal recessive disorder caused by a deficiency of the enzyme uroporphyrinogen cosynthetase, which is important for heme synthesis.

Uroporphyrin 1 and coproporphyrin 1 accumulate in red cells, bone marrow, and other tissues and are deposited in teeth and bone. In the presence of visible light in the Soret band (400-410 nm) and oxygen, uro- and coproporphyrin 1 release energy, and the resultant reactive oxygen species damage tissues.

The gene for uroporphyrinogen cosynthetase is found on chromosome 10. Various gene mutations have been identified, and these affect enzyme function to a greater or lesser degree. The degree of enzyme activity will determine the clinical phenotype seen.

Red urine in infancy may be the first sign of Gunther disease. Severe photosensitivity is encountered in early childhood, leading to friable skin, bulla formation, and subsequent scarring. Bulla fluid may have a reddish tinge. Repeated episodes of scarring lead to loss of acral areas including digits and the tip of the nose and ears (photomutilation). This is accompanied by hemolytic anemia and splenomegaly. Other signs of Gunther disease include red teeth (erythrodontia due to porphyrin deposition) and eye involvement, which may include photosensitivity, keratoconjunctivitis, corneal ulceration, and cataracts, and may lead to blindness. Hypertrichosis may be present. Shortened stature can be a consequence of the disease. 

In the most severe form, Gunther disease causes hemolytic anemia, and hydrops fetalis may occur in utero. A milder form has been recognized where symptoms do not present until later childhood or adulthood.

Codes

ICD10CM:
E80.0 – Hereditary erythropoietic porphyria

SNOMEDCT:
22935002 – Congenital erythropoietic porphyria

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Last Updated:07/19/2023
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Congenital erythropoietic porphyria in Adult
A medical illustration showing key findings of Congenital erythropoietic porphyria (Mild Adult Onset) : Hemolytic anemia, Photodistributed, PLT decreased, Severe photosensitivity
Clinical image of Congenital erythropoietic porphyria - imageId=1691868. Click to open in gallery.  caption: 'Tiny round crusts and erythematous macules and patches on the cheek.'
Tiny round crusts and erythematous macules and patches on the cheek.
Copyright © 2024 VisualDx®. All rights reserved.