Fabry′s disease is an X-linked multisystem disorder due to the deficiency of lysosomal enzyme α-galactosidase A, leads to accumulation of sphingolipids throughout the body. Key causes for premature death include cardiac and renal. Here, we present important clinical findings of such rare case
Fabry disease, a rare X-linked lysosomal storage disorder, is caused by deficiency of the enzyme α-g...
Fabry disease is a rare X-linked recessive lysosomal storage disease, which can cause a wide range o...
International audienceFabry disease (FD) (OMIM 301 500) is a lysosomal storage disorder linked to a ...
Fabry disease is a multisystemic lysosomal storage disorder, inherited in an X-linked manner. It is ...
Fabry disease (FD, OMIM 301500) is a rare X-linked lysosomal storage disorder of the glycosphigolipi...
Fabry disease is a rare X-linked recessive lysosomal storage disease, which can cause a wide range o...
PubMed ID: 28902648Fabry disease is a rare, X-linked, lysosomal glycosphingolipid storage disorder. ...
WOS: 000418480100011PubMed ID: 28902648Fabry disease is a rare, X-linked, lysosomal glycosphingolipi...
Fabry disease (FD) is a rare X-linked lysosomal storage disease with a deficiency of α-galactosidase...
Anderson Fabry disease is a life threatening, X-linked inborn metabolic defect of the lysosomal enzy...
Fabry disease is a lysosomal storage disorder with an X-linked pattern of inheritance. Fabry disease...
Pathogenesis: Fabry disease is an inherited lysosomal storage disorder caused by deficiency of the e...
Fabry disease (FD) is a hereditary metabolic disorder caused by the partial or total inactivation of...
Fabry disease (FD) is a progressive, X-linked lysosomal storage disorder caused by a deficiency of α...
Fabry disease (FD) is a rare, X-linked lysosomal storage disorder resulting in decreased or absent a...
Fabry disease, a rare X-linked lysosomal storage disorder, is caused by deficiency of the enzyme α-g...
Fabry disease is a rare X-linked recessive lysosomal storage disease, which can cause a wide range o...
International audienceFabry disease (FD) (OMIM 301 500) is a lysosomal storage disorder linked to a ...
Fabry disease is a multisystemic lysosomal storage disorder, inherited in an X-linked manner. It is ...
Fabry disease (FD, OMIM 301500) is a rare X-linked lysosomal storage disorder of the glycosphigolipi...
Fabry disease is a rare X-linked recessive lysosomal storage disease, which can cause a wide range o...
PubMed ID: 28902648Fabry disease is a rare, X-linked, lysosomal glycosphingolipid storage disorder. ...
WOS: 000418480100011PubMed ID: 28902648Fabry disease is a rare, X-linked, lysosomal glycosphingolipi...
Fabry disease (FD) is a rare X-linked lysosomal storage disease with a deficiency of α-galactosidase...
Anderson Fabry disease is a life threatening, X-linked inborn metabolic defect of the lysosomal enzy...
Fabry disease is a lysosomal storage disorder with an X-linked pattern of inheritance. Fabry disease...
Pathogenesis: Fabry disease is an inherited lysosomal storage disorder caused by deficiency of the e...
Fabry disease (FD) is a hereditary metabolic disorder caused by the partial or total inactivation of...
Fabry disease (FD) is a progressive, X-linked lysosomal storage disorder caused by a deficiency of α...
Fabry disease (FD) is a rare, X-linked lysosomal storage disorder resulting in decreased or absent a...
Fabry disease, a rare X-linked lysosomal storage disorder, is caused by deficiency of the enzyme α-g...
Fabry disease is a rare X-linked recessive lysosomal storage disease, which can cause a wide range o...
International audienceFabry disease (FD) (OMIM 301 500) is a lysosomal storage disorder linked to a ...