P488: Tandem referral model improves genetic counseling access and efficiency in a kidney genetics clinic*

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Authors: Natalie Vena, Kelsie Bogyo, Kiara I Demorla Ozuna, Simone Sanna‐Cherchi, Krzysztof Kiryluk
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Abstract

Broad-based multigene panel testing is increasingly accessible across medical specialties, changing how patients access genomic services. In emerging specialty genetic clinics, such as nephrogenetics, non-genetics clinicians are ordering genetic tests independently, creating a greater need for expert interpretation and downstream counseling. As a result, the traditional genetic service delivery model, centered on a comprehensive pre- and post-test evaluation following a clinician-initiated referral, is no longer a sustainable or scalable model for care.

Fields of Study & Subjects

Genomics and Rare Diseases Healthcare Systems and Technology Prenatal Screening and Diagnostics

Publication details

Journal / source
Genetics in Medicine Open
Volume
4
Pages
103980–103980
Publication date
1 January 2026
Language
EN