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

Key Clinical Message 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, never been reported before. Therefore, screening i...

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Bibliographic Details

Published in:	Clinical Case Reports
Main Authors:	Yasmine Elsherif, Ismail A. Ibrahim, Omar Elsherif, Hana J. Abukhadijah
Format:	Article
Language:	English
Published:	Wiley 2024-10-01
Subjects:	Anderson‐Fabry disease CDA type II congenital dyserythropoietic anemia co‐occurrence genetic distinction lysosomal disorder
Online Access:	https://doi.org/10.1002/ccr3.9354