← brief for 2026-08-19 · Slowing decline

Less than One in a Million, a Rare Case of Sensenbrenner Syndrome

Key takeaways

This case report describes a rare genetic syndrome with kidney involvement. It used 1 patient over 2 years.

Who did this work

Natalia Lekston (Medical University of Silesia) · Karolina Krzywiecka (Medical University of Silesia) · Natalia Pilśniak (Medical University of Silesia) · Katarzyna Sedlaczek (Medical University of Silesia) · Agnieszka Jędzura (Medical University of Silesia) · Piotr Adamczyk (Medical University of Silesia)

Source

Paper · OpenAlex, CKD works · 2026-08-18
https://doi.org/10.1007/s40142-026-00263-4