Sección: Congenital Defects
Methylmalonic Acidemia with Homocystinuria Type CbLC
Methylmalonic acidemia with homocystinuria is a congenital error in metabolism, consisting of an inability to convert vitamin B12 (cobalamin) into its
Retinal dystrophy associated with mutation in the HK1 gene
Retinitis pigmentosa is a diffuse and hereditary retinal dystrophy that affects photoreceptors, initially rods and later cones (rod-cone dystrophy). T

