Congenital Insensitivity to Pain: A Case Report and Review of the Literature
Figure 1
Image showing the homozygous variant on chromosome 2. (a) Image identifying the homozygous A/A mutation on chromosome 2 at position 167133579 using the DNA nexus platform. (b) Image showing the homozygous c. G2755T mutation in exon 15 of SCN9A gene following amplification and Sanger’s sequencing.
