Analysis of the prevalence and incidence of pseudohypoparathyroidism in Poland based on National Health Fund data with clinical presentation of own cases
In order to quickly establish the correct diagnosis, it is crucial to collect detailed medical interviews with a family history of the disease. It is also essential to carefully perform a physical examination, looking for non-specific symptoms. It's also important to check a broader panel of biochemical tests at the beginning of the diagnosis, characterizing calcium-phosphate homeostasis rather than just the concentration of total calcium in serum.
Authors
- Renata Stawerska (ORCID: https://orcid.org/0000-0002-0508-2186)
- Agnieszka Gach (ORCID: https://orcid.org/0000-0002-6590-5797)
- Elżbieta Skowrońska‐Jóźwiak (ORCID: https://orcid.org/0000-0002-0019-4269)
- Małgorzata Karbownik‐Lewińska (ORCID: https://orcid.org/0000-0002-3045-5669)
- Katarzyna Wojciechowska (ORCID: https://orcid.org/0000-0002-5901-8569)
- Andrzej Lewiñski (ORCID: https://orcid.org/0000-0002-8748-3337)
- Anna Łupińska (ORCID: https://orcid.org/0000-0002-6697-5877)
- Arkadiusz Zygmunt (ORCID: https://orcid.org/0000-0003-2941-8868)
- Monika Pacocha
- Agnieszka Domanska-Czajka
Institutions
- Medical University of Lodz (PL)
- Polish Mother’s Memorial Hospital Research Institute (PL)
Publication Details
- Journal
- Frontiers in Endocrinology
- Published
- 2025-05-15
- DOI
- https://doi.org/10.3389/fendo.2025.1584154
- Citations
- 3
- Primary Topic
- Genetic Syndromes and Imprinting
- Type
- article
- Field-Weighted Citation Impact
- 5.45