Congenital anemia registry for congenital dyserythropoietic anemia
Part of Blood & lymphatic, Genetic & congenital clinical trials.
This study is a registry that collects medical and lab information from people with congenital dyserythropoietic anemia (CDA), a lifelong type of anemia that can cause jaundice. It helps doctors better understand the condition and its causes, including in families where it runs.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have been diagnosed with congenital dyserythropoietic anemia (CDA), even if genetic testing didn’t find a mutation
- You have signs of lifelong anemia or jaundice, or a family member with confirmed CDA
- Your doctor has evidence that your body is not making and using red blood cells effectively (ineffective erythropoiesis)
- Your bone marrow cell appearance (erythroblasts) matches what is typical for CDA
- You do not have a cancer or myelodysplasia (a bone marrow disorder)
- Your anemia is not caused by something else like vitamin B12 deficiency or a medication side effect
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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