How is Congenital Dyserythropoietic Anemia Diagnosed?
Diagnosis of CDA typically involves a combination of clinical evaluation, family history, and specialized tests. These tests may include:
Complete Blood Count (CBC): To detect anemia and other blood abnormalities. Bone Marrow Examination: To identify characteristic morphological abnormalities in erythroblasts. Genetic Testing: To confirm the presence of mutations associated with CDA. HAM's Test: Used specifically for diagnosing CDA Type II.
