Work

Expanding the Genetic Landscape of Congenital Insensitivity to Pain

Year: 2026

Type: article

Abstract: Objectives: , underlie the condition. We investigated the molecular basis of CIP in 2 unrelated families. Methods: Trio whole-exome sequencing was performed for 3 CIP patients from 2 unrelated families and their parents; 1 family with negative results subsequently underwent whole genome sequencing. Sanger sequencing and fluorescent PCR confirmed and sized a GCC repeat expansion. Results: polyalanine expansion reported to date. In Family 2, the proband carried 2 compound-heterozygous variants c.570+2T > G and c.796A > C (p.Thr266Pro) classified as pathogenic and likely pathogenic, respectively, and both previously undescribed. Discussion: as a key gene in pain perception. They also emphasize that diagnostic analysis should target both single-nucleotide variants and polyalanine expansions, which are often underrepresented in whole-exome or whole-genome sequencing data.

Source: Neurology Genetics

DOI: 10.1212/nxg.0000000000200346