by Remember The Girls | Aug 3, 2022
Back to Previous Fabry disease Fabry disease is a rare inherited disorder of glycosphingolipid (fat) metabolism resulting from the absent or markedly deficient activity of the lysosomal enzyme, α-galactosidase A (α-Gal A). This enzymatic deficiency is caused by...
by Remember The Girls | Aug 1, 2022
Back to Previous FG1 Syndrome FG syndrome (FGS) is a genetic condition that affects many parts of the body and occurs almost exclusively in males. FG represents the surname initials of the first individuals diagnosed with the disorder. People with FG syndrome...
by Remember The Girls | Aug 1, 2022
Back to Previous Fragile X Syndrome Fragile X syndrome is characterized by moderate intellectual disability in affected males and mild intellectual disability in affected females. Distinctive physical features are sometimes present in affected males including a large...
