Precise diagnosis of immune-related disorders is the basis for establishing life-changing treatment and management options. By leveraging CentoMD®, our robust mutation database for rare diseases, we carefully curate and document all variants that have clinical relevance for related symptoms – providing the most comprehensive diagnosis of immune-related diseases.
Bone marrow failure/anemia panel
Our bone marrow failure/anemia panel is intended for patients with abnormalities in more than 2 blood cell types (red blood cell, white blood cell, and platelets) who present symptoms of lethargy, recurrent infections, excessive bleeding, abnormal pigmentation, enlarged spleen, and malignancies. Some specific disorders detected with this panel are hemophagocytic lymphohistiocytosis, Seckel syndrome, thrombocytopenia, Fanconi anemia, dyskeratosis congenita, Shwachman Diamond syndrome as well as other types of anemias, such as thalassemia alpha and beta, sickle cell disease, spherocytosis, megaloblastic anemia, congenital sideroblastic, and dyserythropoietic anemia.
|No. of genes:||155|
COMMON SYNDROMES AND DISORDERS COVERED
Bone marrow failure syndrome
Congenital dyserythropoietic anemia
Congenital sideroblastic anemia
CentoImmuno is our solution for immunodeficiency and SCID disorders. Our panel includes genes targeting severe combined immunodeficiency, congenital neutropenia, primary antibody deficiency, common variable immune deficiency, chronic granulomatous disease, autoimmune lymphoproliferative, and agammaglobulinemia.
|No. of genes:||149|