Fabry disease

Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterized by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations.

Anemia

A reduction in erythrocytes volume or hemoglobin concentration.


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PMID (PMCID)
8051496
 MALE Adult
A case of Fabry disease (alpha-galactosidase A deficiency).
Thornbury WC Jr, Aaron P.
J Ky Med Assoc. 1994;92(6):222-6.
The anemia was determined to be of renal origin, and led to a diagnosis of Fabry disease.