OSLAM syndrome

OSLAM syndrome is characterized by the association of osteosarcoma, limb anomalies (clinodactyly with brachymesophalangy, bilateral radioulnar synostosis and absence of one digital ray of the foot) and red cell macrocytosis without anemia.

Also known as: OSLAM syndrome, osteosarcoma-limb anomalies-erythroid macrocytosis syndrome, osteosarcoma, limb anomalies (clinodactyly, absence of digital ray in foot, bilateral radioulnar synostosis) and macrocytosis without anaemia, osteosarcoma, limb anomalies (clinodactyly, absence of digital ray in foot, bilateral radioulnar synostosis) and macrocytosis without anemia, osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow, osteosarcoma, limb anomalies, and macrocytosis

1436 clinical trials for this condition and its sub-types, 0 tagged with OSLAM syndrome itself.