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Chronic Liver Disease in Patients with Prolidase Deficiency: A Case Series.

ABSTRACT:

Introduction

Prolidase deficiency is a rare autosomal recessive disorder caused by variants in the PEPD gene. Patients usually have multi-organ involvement and a wide range of clinical features including recurrent skin ulcers, dysmorphic facial features, recurrent infections, intellectual disability, and splenomegaly. Studies have shown that patients with prolidase deficiency may have hepatic manifestations including hepatomegaly and abnormal liver enzymes. However, there is no detailed description of liver disease in this patient population.

Case presentation

Here, we present 3 patients with prolidase deficiency with varying extents of hepatic involvement.

Conclusion

Prolidase deficiency patients with liver disease should be followed up long term to understand more about the pathophysiology and the impact of liver disease on long-term outcomes.

SUBMITTER: Gopalakrishna H

PROVIDER: S-EPMC10834036 | biostudies-literature | 2024 Jan-Dec

REPOSITORIES: biostudies-literature

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Chronic Liver Disease in Patients with Prolidase Deficiency: A Case Series.

Gopalakrishna Harish H Asif Bilal B Rai Anjali A Conjeevaram Hari S HS Mironova Maria M Kleiner David E DE Freeman Alexandra F AF Heller Theo T

Case reports in gastroenterology 20240101 1

<h4>Introduction</h4>Prolidase deficiency is a rare autosomal recessive disorder caused by variants in the <i>PEPD</i> gene. Patients usually have multi-organ involvement and a wide range of clinical features including recurrent skin ulcers, dysmorphic facial features, recurrent infections, intellectual disability, and splenomegaly. Studies have shown that patients with prolidase deficiency may have hepatic manifestations including hepatomegaly and abnormal liver enzymes. However, there is no de ...[more]

PMID: 38304571

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