The unlikely combination: Anderson–Fabry disease and congenital dyserythropoietic anemia type II in a pediatric patient
<h3>Key Clinical Message</h3><p dir="ltr">Anderson‐Fabry disease, a rare X‐linked lysosomal disorder, and congenital dyserythropoietic anemia (CDA) Type II, an autosomal recessive condition, both have distinct inheritance patterns. Their co‐occurrence is extremely rare, n...
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2024
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