CD40LG and Miyoshi myopathy: H-MM is a numerical chromosomalabnormality associated with a favorableprognosis and better response to treatment (43, 44).There is high platelet count and bone involvementin H-MM patients, but the level of serum markersof bone diseases such as bone alkaline phosphatase(BAP), carboxy-terminal telopeptide of type I collagen(ICTP), osteocalcin (OC), carboxy-terminalpropeptide of type I collagen (PICP) and tartrateresistantacid phosphatase (TRAP) is similar tonon-H-MM patients.