Congenital erythropoietic porphyria: the overlooked inherited disorder

Congenital erythropoietic porphyria (CEP) also known as Gunther's disease is a subtype of porphyria. It is an autosomal recessive disorder caused by a mutation in the uroporphyrinogen III gene (URO III) coding for the enzyme UROS synthase, an essential enzyme in the heme synthesis pathway. The condition may present as non-immune hydrops in foetuses, dark-red urine-stained diapers in neonates and skin blistering and mutilation in sun-exposed areas in older children. Enzyme assays and genetic studies are costly and not easily available in low-resource settings; therefore, awareness of the typical phenotype of this rare porphyria is crucial. However, due to the scarcity of reported cases, clinicians remain oblivious to the disease, leading to delays in diagnosis and initiation of treatment, thus contributing to long-term disabilities. We report a case of a male child in early adolescence presenting with classical cutaneous, skeletal and haematological features of CEP.

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Journal
BMJ Case Reports
Published
2025-03-01
DOI
https://doi.org/10.1136/bcr-2025-264795
Primary Topic
Porphyrin Metabolism and Disorders
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article
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article

Congenital erythropoietic porphyria: the overlooked inherited disorder

Amit Shukla, Anish Upadhyaya, Bhanu Prasad, Mritunjay Kumar et al.
BMJ Case Reports
Porphyrin Metabolism and Disorders
article

Congenital erythropoietic porphyria: the overlooked inherited disorder

Amit Shukla, Anish Upadhyaya, Bhanu Prasad, Mritunjay Kumar, Namita Mishra
article en

Abstract

Congenital erythropoietic porphyria (CEP) also known as Gunther's disease is a subtype of porphyria. It is an autosomal recessive disorder caused by a mutation in the uroporphyrinogen III gene (URO III) coding for the enzyme UROS synthase, an essential enzyme in the heme synthesis pathway. The condition may present as non-immune hydrops in foetuses, dark-red urine-stained diapers in neonates and skin blistering and mutilation in sun-exposed areas in older children. Enzyme assays and genetic studies are costly and not easily available in low-resource settings; therefore, awareness of the typical phenotype of this rare porphyria is crucial. However, due to the scarcity of reported cases, clinicians remain oblivious to the disease, leading to delays in diagnosis and initiation of treatment, thus contributing to long-term disabilities. We report a case of a male child in early adolescence presenting with classical cutaneous, skeletal and haematological features of CEP.

BMJ Case ReportsVol. 18(3)
All India Institute of Medical Sciences (IN)
Quality Education
Openalex Percentile: Top 96%
Porphyrin Metabolism and Disorders
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Congenital erythropoietic porphyria: the overlooked inherited disorder — Amit Shukla, Anish Upadhyaya, et al. · BMJ Case Reports (2025) | TGRS Research Map | TGRS