Rheumatological complaints in H syndrome: from inflammatory profiling to target treatment in a case study

H Syndrome is a rare genetic condition caused by biallelic pathogenic variants in the SLC29A3 gene. It is characterized by a wide range of clinical manifestations, many of which are related to the immune-rheum...
Source: Pediatric Rheumatology - Category: Rheumatology Authors: Tags: Case Report Source Type: research