Add to ORKGFabry disease (Anderson-Fabry disease) is an X-linked recessive lysosomal storage disorder resulting from deficient activity of lysosomal hydrolase, α-galactosidase A (α-Gal A), which leads to progressive accumulation of globotriaosylceramide (Gb3) in various cells, predominantly endothelial and vascular smooth muscle cells, with clinical manifestations affecting major organs including the central nervous system. The incidence has been estimated to 1 per 40,000-60,000 males and 1 per 117,000 in the general population. Symptoms usually occur during childhood or adolescence, occasionally in middle age (according to the level of the enzyme activity). Life-threatening complications often develop in untreated patients. In classic Fabry disease, ...
Background: Fabry disease (FD) is a hereditary metabolic disorder caused by the partial or total ina...
Fabry’s disease is a recessive X -linked disorder that results from a deficiency of the hydrolase al...
Fabry disease, a rare X-linked lysosomal storage disorder, is caused by deficiency of the enzyme α-g...
Fabry disease (Anderson-Fabry disease) is an X-linked recessive lysosomal storage disorder resulting...
SUMMARY – Fabry disease (Anderson-Fabry disease) is an X-linked recessive lysosomal sto-rage disorde...
Fabry's disease is a genetic disorder of X-linked inheritance caused by mutations in the alpha galac...
Fabry disease is an X-linked lysosomal disorder that results from a deficiency of the lysosomal enzy...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by a deficiency of the enzym...
Fabry disease (FD) is a lysosomal storage disorder where deficient or completely absent activity of ...
Fabry disease: Diagnosis and treatment. Fabry disease is an X-linked lysosomal storage disorder that...
Fabry disease (Anderson–Fabry disease) is an X-linked recessive lysosomal storage disorder resulting...
Anderson-Fabry disease is an X-linked recessive glycolipid storage disease caused by deficient activ...
Anderson-Fabry disease (FD) is a rare, progressive, multisystem storage disorder caused by the parti...
Anderson-Fabry disease (FD) is a rare, progressive, multisystem storage disorder caused by the parti...
Fabry disease is a rare, X-linked inborn error of glycosphingolipid catabolism caused by a deficienc...
Background: Fabry disease (FD) is a hereditary metabolic disorder caused by the partial or total ina...
Fabry’s disease is a recessive X -linked disorder that results from a deficiency of the hydrolase al...
Fabry disease, a rare X-linked lysosomal storage disorder, is caused by deficiency of the enzyme α-g...
Fabry disease (Anderson-Fabry disease) is an X-linked recessive lysosomal storage disorder resulting...
SUMMARY – Fabry disease (Anderson-Fabry disease) is an X-linked recessive lysosomal sto-rage disorde...
Fabry's disease is a genetic disorder of X-linked inheritance caused by mutations in the alpha galac...
Fabry disease is an X-linked lysosomal disorder that results from a deficiency of the lysosomal enzy...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by a deficiency of the enzym...
Fabry disease (FD) is a lysosomal storage disorder where deficient or completely absent activity of ...
Fabry disease: Diagnosis and treatment. Fabry disease is an X-linked lysosomal storage disorder that...
Fabry disease (Anderson–Fabry disease) is an X-linked recessive lysosomal storage disorder resulting...
Anderson-Fabry disease is an X-linked recessive glycolipid storage disease caused by deficient activ...
Anderson-Fabry disease (FD) is a rare, progressive, multisystem storage disorder caused by the parti...
Anderson-Fabry disease (FD) is a rare, progressive, multisystem storage disorder caused by the parti...
Fabry disease is a rare, X-linked inborn error of glycosphingolipid catabolism caused by a deficienc...
Background: Fabry disease (FD) is a hereditary metabolic disorder caused by the partial or total ina...
Fabry’s disease is a recessive X -linked disorder that results from a deficiency of the hydrolase al...
Fabry disease, a rare X-linked lysosomal storage disorder, is caused by deficiency of the enzyme α-g...