The unlikely combination: Anderson–Fabry disease and congenital dyserythropoietic anemia type II in a pediatric patient

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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Bibliographic Details
Main Author: Yasmine Elsherif (22045415) (author)
Other Authors: Ismail A. Ibrahim (17687436) (author), Omar Elsherif (4164418) (author), Hana J. Abukhadijah (22045418) (author)
Published: 2024
Subjects:
Biological sciences
Genetics
Biomedical and clinical sciences
Clinical sciences
Paediatrics
Anderson- Fabry disease
CDA type II
congenital dyserythropoietic anemia
co-occurrence
genetic distinction
lysosomal disorder
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