Evidence map›Paper›PMID 40502951›Full record

ArticleEuropean journal of case reports in internal medicine2025

Successful Pregnancy Outcome in Patient with Pompe Disease Despite Discontinuation of Enzyme Replacement Therapy.

Dunja Leskovar Lemešić, Dražen Perica, Gordan Zlopaša, Biserka Knezić Frković, Nediljko Šućur, Željko Reiner, Ivan Pećin

Abstract read
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Article in European journal of case reports in internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Dunja Leskovar LemešićDivision for Metabolic Diseases, Department of Internal Medicine, University Hospital Centre Zagreb, Zagreb, Croatia.
Dražen PericaDivision for Metabolic Diseases, Department of Internal Medicine, University Hospital Centre Zagreb, Zagreb, Croatia.
Gordan ZlopašaDepartment of Obstetrics and Gynecology, University Hospital Centre Zagreb, Zagreb, Croatia.
Biserka Knezić FrkovićDepartment of Obstetrics and Gynecology, University Hospital Centre Zagreb, Zagreb, Croatia.
Nediljko ŠućurDivision for Metabolic Diseases, Department of Internal Medicine, University Hospital Centre Zagreb, Zagreb, Croatia.
Željko ReinerDivision for Metabolic Diseases, Department of Internal Medicine, University Hospital Centre Zagreb, Zagreb, Croatia.
Ivan PećinDivision for Metabolic Diseases, Department of Internal Medicine, University Hospital Centre Zagreb, Zagreb, Croatia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pompe disease (PD), is an autosomal recessive metabolic disorder caused by mutations in the acid alpha-glucosidase (GAA) gene, resulting in a deficiency of the same enzyme and glycogen buildup in tissues. Late onset PD (LOPD) is characterized by muscle illness, accompanied by diaphragmatic involvement and leading to respiratory insufficiency. Fortunately, the disease progresses slowly, and treatment with enzyme replacement therapy can further delay its development. Pregnancy in women with LOPD requires special caution because musculoskeletal changes and greater physical demands may worsen muscular weakness and endanger both the mother and unborn child. Although several cases of pregnant women with LOPD that continued enzyme replacement therapy (ERT) during pregnancy have been reported, there is still a lack of data regarding teratogenicity and safety of the foetus. Case report: We present a case of a 31-year-old pregnant women with a mild form of LOPD who discontinued ERT during whole pregnancy. During the whole pregnancy there were no clinical signs of progression of muscle or pulmonary weakness. With careful monitoring of the patient and foetus, and planned delivery, a healthy baby girl was born. ERT was reintroduced 6 months after delivery with premedication (corticosteroids and antihistamines) for the first application, with no allergic reaction noted. Conclusion: In this patient with well-controlled LOPD, ERT was safely discontinued during pregnancy without disease worsening. The risks of ERT in pregnancy outweighed the potential complications of well-controlled disease. The final decision should be made with an individual approach for each patient by a multidisciplinary team. LEARNING POINTS: Pompe disease in pregnancy represents a treatment challenge due to the increased risk of worsening respiratory and muscle function and requires a multidisciplinary approach.Although several case reports reported safe usage of enzyme replacement therapy (ERT) during pregnancy, more studies are needed to address the safety for the foetus and overall teratogenicity.In well controlled Pompe disease, ERT can be discontinued during pregnancy with careful foetal and maternal monitoring.

Indexed as

enzyme replacement therapyLate onset Pompe diseasemuscle weaknesspregnancy

Identifiers

PMID40502951
PMCPMC12151579

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