MYH9-related syndromic thrombocytopenia in Pennsylvania

1 treatment center for MYH9-related syndromic thrombocytopenia in Pennsylvania, verified against ClinicalTrials.gov, PubMed, and the NPPES NPI registry.

MYH9-related syndromic thrombocytopenia (Orphanet code 182050) is a group of rare inherited disorders caused by mutations in the MYH9 gene, which encodes non-muscle myosin heavy chain IIA. This condition encompasses several previously distinct clinical entities, including May-Hegglin anomaly, Epstein syndrome, Fechtner…