Fabry disease is an X-linked inherited condition due to the absence or reduction of alpha-galactosidase activity in lysosomes, that results in accumulation of globotriaosylceramide (Gb3) and related neutral glycosphingolipids. Manifestations of Fabry disease include serious and progressive impairment of renal and cardiac function. In addition, patients experience pain, gastrointestinal disturbance, transient ischaemic attacks and strokes. Additional effects on the skin, eyes, ears, lungs and bones are often seen. The first symptoms of classic Fabry disease usually appear in childhood. Despite being X-linked, females can suffer the same severity of symptoms as males, and life expectancy is reduced in both females and males. Enzyme ...
Fabry disease (FD) is an X-linked inborn error of glycosphingolipid metabolism due to the deficiency...
Fabry disease is a rare, X-linked inborn error of glycosphingolipid catabolism caused by a deficienc...
Fabry disease (FD) is a lysosomal storage disorder (LSD) characterized by the deficiency of alpha-ga...
Fabry disease is an X-linked inherited condition due to the absence or reduction of alpha-galactos...
Fabry disease is an X-linked lysosomal disorder that results from a deficiency of the lysosomal enzy...
Fabry disease is an X-linked inherited lysosomal disorder due to dysfunctions of the lysosomal enzym...
Fabrys disease is a lysosomal storage disorder, caused due to mutation in the GLA gene in X-chromoso...
Fabry disease: Diagnosis and treatment. Fabry disease is an X-linked lysosomal storage disorder that...
Fabry disease is a multisystemic lysosomal storage disorder, inherited in an X-linked manner. It is ...
Fabry disease is a lysosomal storage disorder with an X-linked pattern of inheritance. Fabry disease...
Fabry disease, a rare X-linked lysosomal storage disorder, is caused by deficiency of the enzyme α-g...
Fabry disease (FD) is a rare, X-linked inherited disorder of glycosphingolipid metabolism. It leads ...
Fabry disease is a rare X-linked lysosomal storage disorder due to mutations in the GLA gene causing...
Abstract Background In Fabry disease (α-galactosidase A deficiency) accumulation of Globotriaosylcer...
Pathogenesis: Fabry disease is an inherited lysosomal storage disorder caused by deficiency of the e...
Fabry disease (FD) is an X-linked inborn error of glycosphingolipid metabolism due to the deficiency...
Fabry disease is a rare, X-linked inborn error of glycosphingolipid catabolism caused by a deficienc...
Fabry disease (FD) is a lysosomal storage disorder (LSD) characterized by the deficiency of alpha-ga...
Fabry disease is an X-linked inherited condition due to the absence or reduction of alpha-galactos...
Fabry disease is an X-linked lysosomal disorder that results from a deficiency of the lysosomal enzy...
Fabry disease is an X-linked inherited lysosomal disorder due to dysfunctions of the lysosomal enzym...
Fabrys disease is a lysosomal storage disorder, caused due to mutation in the GLA gene in X-chromoso...
Fabry disease: Diagnosis and treatment. Fabry disease is an X-linked lysosomal storage disorder that...
Fabry disease is a multisystemic lysosomal storage disorder, inherited in an X-linked manner. It is ...
Fabry disease is a lysosomal storage disorder with an X-linked pattern of inheritance. Fabry disease...
Fabry disease, a rare X-linked lysosomal storage disorder, is caused by deficiency of the enzyme α-g...
Fabry disease (FD) is a rare, X-linked inherited disorder of glycosphingolipid metabolism. It leads ...
Fabry disease is a rare X-linked lysosomal storage disorder due to mutations in the GLA gene causing...
Abstract Background In Fabry disease (α-galactosidase A deficiency) accumulation of Globotriaosylcer...
Pathogenesis: Fabry disease is an inherited lysosomal storage disorder caused by deficiency of the e...
Fabry disease (FD) is an X-linked inborn error of glycosphingolipid metabolism due to the deficiency...
Fabry disease is a rare, X-linked inborn error of glycosphingolipid catabolism caused by a deficienc...
Fabry disease (FD) is a lysosomal storage disorder (LSD) characterized by the deficiency of alpha-ga...