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Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2
A sideroblastic anemia that is characterized by microcytic hypochromic anemia and iron overload, and is caused by autosomal recessive inheritance of mutation in the SLC25A38 gene.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
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Overview
A sideroblastic anemia that is characterized by microcytic hypochromic anemia and iron overload, and is caused by autosomal recessive inheritance of mutation in the SLC25A38 gene.
Resources
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