RARE PATHOLOGY OF CHILDHOOD: TAR SYNDROME. A CASE REPORT

The article provides a contemporary literature review on the causes, clinical features, laboratory criteria, and management strategies for children with a rare condition – TAR-syndrome. The review is supported by a clinical case of a disease in an infant girl born with thrombocytopenia and a bilateral absence of the radial bones. The diagnosis was confirmed by a specific cytogenetic and molecular study.