The case for including proteomics in routine diagnostic practice for rare disease
Paediatrics
The case for including proteomics in routine diagnostic practice for rare disease
Paediatrics

The case for including proteomics in routine diagnostic practice for rare disease

Genome Med. 2025 May 26;17(1):61. doi: 10.1186/s13073-025-01491-z.

ABSTRACT

Many people with rare diseases cannot access personalized therapies because they do not have a confirmed genetic diagnosis. Promising technologies including proteomics are underutilized in routine diagnostic practice. It is time to incorporate proteomics into the diagnostic workflow to shorten time to diagnosis and expand treatment options for rare disease.

PMID:40420250 | DOI:10.1186/s13073-025-01491-z